Canonical Allele Identifier: CA354229113
Gene: MYLK HGNC NCBI
MYLK-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123614263C>T , CM000665.2:g.123614263C>T GRCh38
NC_000003.11:g.123333110C>T , CM000665.1:g.123333110C>T GRCh37
NC_000003.10:g.124815800C>T NCBI36
NG_029111.1:g.275040G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.5227G>A (MYLK) ENSP00000320622.6:p.Gly1743Arg
ENST00000508240.2:c.1987G>A (MYLK) ENSP00000422984.2:p.Gly663Arg
ENST00000578202.2:c.*92G>A (MYLK) ENSP00000463691.2:n.*92G>A
ENST00000583087.6:c.307G>A (MYLK) ENSP00000462118.1:p.Gly103Arg
ENST00000685021.1:c.2821G>A (MYLK) ENSP00000508447.1:p.Gly941Arg
ENST00000685170.1:n.800G>A (MYLK)
ENST00000685259.1:c.3106G>A (MYLK)
ENST00000685744.1:c.304G>A (MYLK) ENSP00000510047.1:p.Gly102Arg
ENST00000685907.1:n.3368G>A (MYLK)
ENST00000685953.1:c.1984G>A (MYLK) ENSP00000510593.1:p.Gly662Arg
ENST00000686039.1:c.2971G>A (MYLK)
ENST00000686245.1:c.2704G>A (MYLK) ENSP00000509313.1:p.Gly902Arg
ENST00000686281.1:n.879G>A (MYLK)
ENST00000686406.1:c.5584G>A (MYLK) ENSP00000509044.1:p.Gly1862Arg
ENST00000686458.1:n.2089G>A (MYLK)
ENST00000686761.1:c.5587G>A (MYLK) ENSP00000508758.1:p.Gly1863Arg
ENST00000687375.1:c.304G>A (MYLK) ENSP00000509867.1:p.Gly102Arg
ENST00000687434.1:c.*1803G>A (MYLK) ENSP00000509751.1:n.*1803G>A
ENST00000687709.1:n.3642G>A (MYLK)
ENST00000687848.1:c.5617G>A (MYLK) ENSP00000508761.1:p.Gly1873Arg
ENST00000688024.1:c.2818G>A (MYLK) ENSP00000509803.1:p.Gly940Arg
ENST00000688223.1:c.2617G>A (MYLK) ENSP00000508935.1:p.Gly873Arg
ENST00000689446.1:n.789G>A (MYLK)
ENST00000689868.1:n.5847G>A (MYLK)
ENST00000689918.1:n.1662G>A (MYLK)
ENST00000690086.1:n.1688G>A (MYLK)
ENST00000690167.1:n.3255G>A (MYLK)
ENST00000690457.1:c.4825G>A (MYLK) ENSP00000508777.1:p.Gly1609Arg
ENST00000690534.1:n.2108G>A (MYLK)
ENST00000690656.1:n.292G>A (MYLK)
ENST00000691367.1:n.283G>A (MYLK)
ENST00000691933.1:c.3211G>A (MYLK)
ENST00000692356.1:c.89-151G>A (MYLK) ENSP00000509805.1:n.89-151G>A
ENST00000692507.1:n.1391G>A (MYLK)
ENST00000693689.1:c.5380G>A (MYLK) ENSP00000510503.1:p.Gly1794Arg
ENST00000360304.8:c.5587G>A (MYLK) MANE Select ENSP00000353452.3:p.Gly1863Arg
ENST00000346322.9:c.5380G>A (MYLK) ENSP00000320622.5:p.Gly1794Arg
ENST00000354792.9:c.5380G>A (MYLK) ENSP00000346846.6:p.Gly1794Arg
ENST00000359169.5:c.5434G>A (MYLK) ENSP00000352088.1:p.Gly1812Arg
ENST00000360304.7:c.5587G>A (MYLK) ENSP00000353452.3:p.Gly1863Arg
ENST00000360772.7:c.5434G>A (MYLK) ENSP00000354004.3:p.Gly1812Arg
ENST00000418370.6:c.307G>A (MYLK) ENSP00000428967.1:p.Gly103Arg
ENST00000464489.5:c.*5166G>A (MYLK) ENSP00000417798.1:n.*5166G>A
ENST00000475616.5:c.5587G>A (MYLK) ENSP00000418335.1:p.Gly1863Arg
ENST00000578202.1:c.304G>A (MYLK) ENSP00000463691.1:p.Gly102Arg
ENST00000583087.5:c.307G>A (MYLK) ENSP00000462118.1:p.Gly103Arg
NM_053025.3:c.5587G>A (MYLK) NP_444253.3:p.Gly1863Arg
NM_053026.3:c.5380G>A (MYLK) NP_444254.3:p.Gly1794Arg
NM_053027.3:c.5434G>A (MYLK) NP_444255.3:p.Gly1812Arg
NM_053028.3:c.5227G>A (MYLK) NP_444256.3:p.Gly1743Arg
NM_053031.2:c.304G>A (MYLK) NP_444259.1:p.Gly102Arg
NM_053032.2:c.307G>A (MYLK) NP_444260.1:p.Gly103Arg
NR_038266.2:n.290-15231C>T (MYLK-AS1)
NR_121654.1:n.197-15231C>T (MYLK-AS1)
XM_011512860.1:c.5584G>A (MYLK) XP_011511162.1:p.Gly1862Arg
XM_011512861.1:c.5383G>A (MYLK) XP_011511163.1:p.Gly1795Arg
XM_011512862.1:c.5059G>A (MYLK) XP_011511164.1:p.Gly1687Arg
NM_001321309.1:c.5059G>A (MYLK) NP_001308238.1:p.Gly1687Arg
NM_053031.3:c.304G>A (MYLK) NP_444259.1:p.Gly102Arg
NM_053032.3:c.307G>A (MYLK) NP_444260.1:p.Gly103Arg
XM_011512860.3:c.5614G>A (MYLK) XP_011511162.2:p.Gly1872Arg
XM_011512861.3:c.5413G>A (MYLK) XP_011511163.2:p.Gly1805Arg
XM_017006469.2:c.2818G>A (MYLK) XP_016861958.1:p.Gly940Arg
XM_017006470.2:c.1984G>A (MYLK) XP_016861959.1:p.Gly662Arg
XM_017006471.2:c.1987G>A (MYLK) XP_016861960.1:p.Gly663Arg
XM_017006472.2:c.307G>A (MYLK) XP_016861961.1:p.Gly103Arg
XM_017006473.1:c.304G>A (MYLK) XP_016861962.1:p.Gly102Arg
XM_024453532.1:c.5617G>A (MYLK) XP_024309300.1:p.Gly1873Arg
XM_024453533.1:c.5587G>A (MYLK) XP_024309301.1:p.Gly1863Arg
XM_024453534.1:c.5410G>A (MYLK) XP_024309302.1:p.Gly1804Arg
XM_024453535.1:c.5380G>A (MYLK) XP_024309303.1:p.Gly1794Arg
XM_024453536.1:c.5587G>A (MYLK) XP_024309304.1:p.Gly1863Arg
XM_024453537.1:c.5587G>A (MYLK) XP_024309305.1:p.Gly1863Arg
NM_001321309.2:c.5059G>A (MYLK) NP_001308238.1:p.Gly1687Arg
NM_053025.4:c.5587G>A (MYLK) MANE Select NP_444253.3:p.Gly1863Arg
NM_053026.4:c.5380G>A (MYLK) NP_444254.3:p.Gly1794Arg
NM_053027.4:c.5434G>A (MYLK) NP_444255.3:p.Gly1812Arg
NM_053028.4:c.5227G>A (MYLK) NP_444256.3:p.Gly1743Arg
NM_053031.4:c.304G>A (MYLK) NP_444259.1:p.Gly102Arg
NM_053032.4:c.307G>A (MYLK) NP_444260.1:p.Gly103Arg