Canonical Allele Identifier: CA072665
Gene: MYLK HGNC NCBI
MYLK-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123626796T>A , CM000665.2:g.123626796T>A GRCh38
NC_000003.11:g.123345643T>A , CM000665.1:g.123345643T>A GRCh37
NC_000003.10:g.124828333T>A NCBI36
NG_029111.1:g.262507A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.4878+22A>T (MYLK) ENSP00000320622.6:n.4878+22A>T
ENST00000508240.2:c.1638+22A>T (MYLK) ENSP00000422984.2:n.1638+22A>T
ENST00000684879.1:n.2870+22A>T (MYLK)
ENST00000685021.1:c.2472+22A>T (MYLK) ENSP00000508447.1:n.2472+22A>T
ENST00000685170.1:n.451+22A>T (MYLK)
ENST00000685259.1:c.2757+22A>T (MYLK)
ENST00000685907.1:n.3019+22A>T (MYLK)
ENST00000685953.1:c.1638+22A>T (MYLK) ENSP00000510593.1:n.1638+22A>T
ENST00000686039.1:c.2622+22A>T (MYLK)
ENST00000686245.1:c.2355+22A>T (MYLK) ENSP00000509313.1:n.2355+22A>T
ENST00000686281.1:n.530+22A>T (MYLK)
ENST00000686406.1:c.5238+22A>T (MYLK) ENSP00000509044.1:n.5238+22A>T
ENST00000686458.1:n.1740+22A>T (MYLK)
ENST00000686761.1:c.5238+22A>T (MYLK) ENSP00000508758.1:n.5238+22A>T
ENST00000686822.1:n.5132+22A>T (MYLK)
ENST00000687434.1:c.*1454+22A>T (MYLK) ENSP00000509751.1:n.*1454+22A>T
ENST00000687709.1:n.3293+22A>T (MYLK)
ENST00000687848.1:c.5268+22A>T (MYLK) ENSP00000508761.1:n.5268+22A>T
ENST00000688024.1:c.2472+22A>T (MYLK) ENSP00000509803.1:n.2472+22A>T
ENST00000688223.1:c.2268+22A>T (MYLK) ENSP00000508935.1:n.2268+22A>T
ENST00000689446.1:n.443+22A>T (MYLK)
ENST00000689868.1:n.5498+22A>T (MYLK)
ENST00000689918.1:n.1313+22A>T (MYLK)
ENST00000690086.1:n.1339+22A>T (MYLK)
ENST00000690167.1:n.2909+22A>T (MYLK)
ENST00000690457.1:c.4476+22A>T (MYLK) ENSP00000508777.1:n.4476+22A>T
ENST00000690534.1:n.1759+22A>T (MYLK)
ENST00000691933.1:c.2862+22A>T (MYLK)
ENST00000693689.1:c.5031+22A>T (MYLK) ENSP00000510503.1:n.5031+22A>T
ENST00000360304.8:c.5238+22A>T (MYLK) MANE Select ENSP00000353452.3:n.5238+22A>T
ENST00000346322.9:c.5031+22A>T (MYLK) ENSP00000320622.5:n.5031+22A>T
ENST00000354792.9:c.5031+22A>T (MYLK) ENSP00000346846.6:n.5031+22A>T
ENST00000359169.5:c.5085+22A>T (MYLK) ENSP00000352088.1:n.5085+22A>T
ENST00000360304.7:c.5238+22A>T (MYLK) ENSP00000353452.3:n.5238+22A>T
ENST00000360772.7:c.5085+22A>T (MYLK) ENSP00000354004.3:n.5085+22A>T
ENST00000464489.5:c.*4817+22A>T (MYLK) ENSP00000417798.1:n.*4817+22A>T
ENST00000475616.5:c.5238+22A>T (MYLK) ENSP00000418335.1:n.5238+22A>T
NM_053025.3:c.5238+22A>T (MYLK) NP_444253.3:n.5238+22A>T
NM_053026.3:c.5031+22A>T (MYLK) NP_444254.3:n.5031+22A>T
NM_053027.3:c.5085+22A>T (MYLK) NP_444255.3:n.5085+22A>T
NM_053028.3:c.4878+22A>T (MYLK) NP_444256.3:n.4878+22A>T
NR_038266.2:n.290-2698T>A (MYLK-AS1)
NR_121654.1:n.197-2698T>A (MYLK-AS1)
XM_011512860.1:c.5238+22A>T (MYLK) XP_011511162.1:n.5238+22A>T
XM_011512861.1:c.5034+22A>T (MYLK) XP_011511163.1:n.5034+22A>T
XM_011512862.1:c.4710+22A>T (MYLK) XP_011511164.1:n.4710+22A>T
NM_001321309.1:c.4710+22A>T (MYLK) NP_001308238.1:n.4710+22A>T
XM_011512860.3:c.5268+22A>T (MYLK) XP_011511162.2:n.5268+22A>T
XM_011512861.3:c.5064+22A>T (MYLK) XP_011511163.2:n.5064+22A>T
XM_017006469.2:c.2472+22A>T (MYLK) XP_016861958.1:n.2472+22A>T
XM_017006470.2:c.1638+22A>T (MYLK) XP_016861959.1:n.1638+22A>T
XM_017006471.2:c.1638+22A>T (MYLK) XP_016861960.1:n.1638+22A>T
XM_024453532.1:c.5268+22A>T (MYLK) XP_024309300.1:n.5268+22A>T
XM_024453533.1:c.5238+22A>T (MYLK) XP_024309301.1:n.5238+22A>T
XM_024453534.1:c.5061+22A>T (MYLK) XP_024309302.1:n.5061+22A>T
XM_024453535.1:c.5031+22A>T (MYLK) XP_024309303.1:n.5031+22A>T
XM_024453536.1:c.5238+22A>T (MYLK) XP_024309304.1:n.5238+22A>T
XM_024453537.1:c.5238+22A>T (MYLK) XP_024309305.1:n.5238+22A>T
NM_001321309.2:c.4710+22A>T (MYLK) NP_001308238.1:n.4710+22A>T
NM_053025.4:c.5238+22A>T (MYLK) MANE Select NP_444253.3:n.5238+22A>T
NM_053026.4:c.5031+22A>T (MYLK) NP_444254.3:n.5031+22A>T
NM_053027.4:c.5085+22A>T (MYLK) NP_444255.3:n.5085+22A>T
NM_053028.4:c.4878+22A>T (MYLK) NP_444256.3:n.4878+22A>T