Canonical Allele Identifier: CA435431454

Gene: MYLK MYLK-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123614183T>C , CM000665.2:g.123614183T>C	GRCh38
NC_000003.11:g.123333030T>C , CM000665.1:g.123333030T>C	GRCh37
NC_000003.10:g.124815720T>C	NCBI36
NG_029111.1:g.275120A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.5307A>G (MYLK)	ENSP00000320622.6:p.Gly1769=
ENST00000508240.2:c.2067A>G (MYLK)	ENSP00000422984.2:p.Gly689=
ENST00000578202.2:c.*172A>G (MYLK)	ENSP00000463691.2:n.*172A>G
ENST00000583087.6:c.387A>G (MYLK)	ENSP00000462118.1:p.Gly129=
ENST00000685021.1:c.2901A>G (MYLK)	ENSP00000508447.1:p.Gly967=
ENST00000685170.1:n.880A>G (MYLK)
ENST00000685259.1:c.3186A>G (MYLK)
ENST00000685744.1:c.384A>G (MYLK)	ENSP00000510047.1:p.Gly128=
ENST00000685907.1:n.3448A>G (MYLK)
ENST00000685953.1:c.2064A>G (MYLK)	ENSP00000510593.1:p.Gly688=
ENST00000686039.1:c.3051A>G (MYLK)
ENST00000686245.1:c.2784A>G (MYLK)	ENSP00000509313.1:p.Gly928=
ENST00000686281.1:n.959A>G (MYLK)
ENST00000686406.1:c.5664A>G (MYLK)	ENSP00000509044.1:p.Gly1888=
ENST00000686458.1:n.2169A>G (MYLK)
ENST00000686761.1:c.5667A>G (MYLK)	ENSP00000508758.1:p.Gly1889=
ENST00000687375.1:c.384A>G (MYLK)	ENSP00000509867.1:p.Gly128=
ENST00000687434.1:c.*1883A>G (MYLK)	ENSP00000509751.1:n.*1883A>G
ENST00000687709.1:n.3722A>G (MYLK)
ENST00000687848.1:c.5697A>G (MYLK)	ENSP00000508761.1:p.Gly1899=
ENST00000688024.1:c.2898A>G (MYLK)	ENSP00000509803.1:p.Gly966=
ENST00000688223.1:c.2697A>G (MYLK)	ENSP00000508935.1:p.Gly899=
ENST00000689446.1:n.869A>G (MYLK)
ENST00000689868.1:n.5927A>G (MYLK)
ENST00000689918.1:n.1742A>G (MYLK)
ENST00000690167.1:n.3335A>G (MYLK)
ENST00000690457.1:c.4905A>G (MYLK)	ENSP00000508777.1:p.Gly1635=
ENST00000690656.1:n.372A>G (MYLK)
ENST00000691367.1:n.363A>G (MYLK)
ENST00000691933.1:c.3291A>G (MYLK)
ENST00000692356.1:c.89-71A>G (MYLK)	ENSP00000509805.1:n.89-71A>G
ENST00000692507.1:n.1471A>G (MYLK)
ENST00000693689.1:c.5460A>G (MYLK)	ENSP00000510503.1:p.Gly1820=
ENST00000360304.8:c.5667A>G (MYLK) MANE Select	ENSP00000353452.3:p.Gly1889=
ENST00000346322.9:c.5460A>G (MYLK)	ENSP00000320622.5:p.Gly1820=
ENST00000354792.9:c.5460A>G (MYLK)	ENSP00000346846.6:p.Gly1820=
ENST00000359169.5:c.5514A>G (MYLK)	ENSP00000352088.1:p.Gly1838=
ENST00000360304.7:c.5667A>G (MYLK)	ENSP00000353452.3:p.Gly1889=
ENST00000360772.7:c.5514A>G (MYLK)	ENSP00000354004.3:p.Gly1838=
ENST00000418370.6:c.387A>G (MYLK)	ENSP00000428967.1:p.Gly129=
ENST00000464489.5:c.*5246A>G (MYLK)	ENSP00000417798.1:n.*5246A>G
ENST00000475616.5:c.5667A>G (MYLK)	ENSP00000418335.1:p.Gly1889=
ENST00000578202.1:c.384A>G (MYLK)	ENSP00000463691.1:p.Gly128=
ENST00000583087.5:c.387A>G (MYLK)	ENSP00000462118.1:p.Gly129=
NM_053025.3:c.5667A>G (MYLK)	NP_444253.3:p.Gly1889=
NM_053026.3:c.5460A>G (MYLK)	NP_444254.3:p.Gly1820=
NM_053027.3:c.5514A>G (MYLK)	NP_444255.3:p.Gly1838=
NM_053028.3:c.5307A>G (MYLK)	NP_444256.3:p.Gly1769=
NM_053031.2:c.384A>G (MYLK)	NP_444259.1:p.Gly128=
NM_053032.2:c.387A>G (MYLK)	NP_444260.1:p.Gly129=
NR_038266.2:n.290-15311T>C (MYLK-AS1)
NR_121654.1:n.197-15311T>C (MYLK-AS1)
XM_011512860.1:c.5664A>G (MYLK)	XP_011511162.1:p.Gly1888=
XM_011512861.1:c.5463A>G (MYLK)	XP_011511163.1:p.Gly1821=
XM_011512862.1:c.5139A>G (MYLK)	XP_011511164.1:p.Gly1713=
NM_001321309.1:c.5139A>G (MYLK)	NP_001308238.1:p.Gly1713=
NM_053031.3:c.384A>G (MYLK)	NP_444259.1:p.Gly128=
NM_053032.3:c.387A>G (MYLK)	NP_444260.1:p.Gly129=
XM_011512860.3:c.5694A>G (MYLK)	XP_011511162.2:p.Gly1898=
XM_011512861.3:c.5493A>G (MYLK)	XP_011511163.2:p.Gly1831=
XM_017006469.2:c.2898A>G (MYLK)	XP_016861958.1:p.Gly966=
XM_017006470.2:c.2064A>G (MYLK)	XP_016861959.1:p.Gly688=
XM_017006471.2:c.2067A>G (MYLK)	XP_016861960.1:p.Gly689=
XM_017006472.2:c.387A>G (MYLK)	XP_016861961.1:p.Gly129=
XM_017006473.1:c.384A>G (MYLK)	XP_016861962.1:p.Gly128=
XM_024453532.1:c.5697A>G (MYLK)	XP_024309300.1:p.Gly1899=
XM_024453533.1:c.5667A>G (MYLK)	XP_024309301.1:p.Gly1889=
XM_024453534.1:c.5490A>G (MYLK)	XP_024309302.1:p.Gly1830=
XM_024453535.1:c.5460A>G (MYLK)	XP_024309303.1:p.Gly1820=
XM_024453536.1:c.5667A>G (MYLK)	XP_024309304.1:p.Gly1889=
XM_024453537.1:c.5667A>G (MYLK)	XP_024309305.1:p.Gly1889=
NM_001321309.2:c.5139A>G (MYLK)	NP_001308238.1:p.Gly1713=
NM_053025.4:c.5667A>G (MYLK) MANE Select	NP_444253.3:p.Gly1889=
NM_053026.4:c.5460A>G (MYLK)	NP_444254.3:p.Gly1820=
NM_053027.4:c.5514A>G (MYLK)	NP_444255.3:p.Gly1838=
NM_053028.4:c.5307A>G (MYLK)	NP_444256.3:p.Gly1769=
NM_053031.4:c.384A>G (MYLK)	NP_444259.1:p.Gly128=
NM_053032.4:c.387A>G (MYLK)	NP_444260.1:p.Gly129=