Canonical Allele Identifier: CA354233970

Gene: MYLK

Linked Data

• dbSNP Id: rs2108635709
• MyVariant Identifiers: chr3:g.123426748G>C (hg19) ; chr3:g.123707901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123707901G>C , CM000665.2:g.123707901G>C	GRCh38
NC_000003.11:g.123426748G>C , CM000665.1:g.123426748G>C	GRCh37
NC_000003.10:g.124909438G>C	NCBI36
NG_029111.1:g.181402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.2036C>G	ENSP00000320622.6:p.Pro679Arg
ENST00000686406.1:c.2243C>G	ENSP00000509044.1:p.Pro748Arg
ENST00000686761.1:c.2243C>G	ENSP00000508758.1:p.Pro748Arg
ENST00000686822.1:n.2137C>G
ENST00000687848.1:c.2273C>G	ENSP00000508761.1:p.Pro758Arg
ENST00000690457.1:c.1481C>G	ENSP00000508777.1:p.Pro494Arg
ENST00000693689.1:c.2036C>G	ENSP00000510503.1:p.Pro679Arg
ENST00000360304.8:c.2243C>G MANE Select	ENSP00000353452.3:p.Pro748Arg
ENST00000346322.9:c.2036C>G	ENSP00000320622.5:p.Pro679Arg
ENST00000354792.9:c.2036C>G	ENSP00000346846.6:p.Pro679Arg
ENST00000359169.5:c.2243C>G	ENSP00000352088.1:p.Pro748Arg
ENST00000360304.7:c.2243C>G	ENSP00000353452.3:p.Pro748Arg
ENST00000360772.7:c.2243C>G	ENSP00000354004.3:p.Pro748Arg
ENST00000464489.5:c.*1822C>G	ENSP00000417798.1:n.*1822C>G
ENST00000475616.5:c.2243C>G	ENSP00000418335.1:p.Pro748Arg
NM_053025.3:c.2243C>G	NP_444253.3:p.Pro748Arg
NM_053026.3:c.2036C>G	NP_444254.3:p.Pro679Arg
NM_053027.3:c.2243C>G	NP_444255.3:p.Pro748Arg
NM_053028.3:c.2036C>G	NP_444256.3:p.Pro679Arg
XM_011512860.1:c.2243C>G	XP_011511162.1:p.Pro748Arg
XM_011512861.1:c.2243C>G	XP_011511163.1:p.Pro748Arg
XM_011512862.1:c.1715C>G	XP_011511164.1:p.Pro572Arg
XR_241556.2:n.313+3892G>C
XR_427403.2:n.406+3892G>C
XR_924414.1:n.406+3892G>C
XR_924415.1:n.403+3892G>C
XR_924416.1:n.230+3892G>C
XR_924417.1:n.226+3892G>C
XR_924418.1:n.406+3892G>C
NM_001321309.1:c.1715C>G	NP_001308238.1:p.Pro572Arg
XM_011512860.3:c.2273C>G	XP_011511162.2:p.Pro758Arg
XM_011512861.3:c.2273C>G	XP_011511163.2:p.Pro758Arg
XM_024453532.1:c.2273C>G	XP_024309300.1:p.Pro758Arg
XM_024453533.1:c.2243C>G	XP_024309301.1:p.Pro748Arg
XM_024453534.1:c.2066C>G	XP_024309302.1:p.Pro689Arg
XM_024453535.1:c.2036C>G	XP_024309303.1:p.Pro679Arg
XM_024453536.1:c.2243C>G	XP_024309304.1:p.Pro748Arg
XM_024453537.1:c.2243C>G	XP_024309305.1:p.Pro748Arg
XR_001740871.2:n.406+3892G>C
XR_427403.4:n.406+3892G>C
XR_924414.3:n.406+3892G>C
XR_924417.3:n.251+3892G>C
XR_924418.3:n.406+3892G>C
NM_001321309.2:c.1715C>G	NP_001308238.1:p.Pro572Arg
NM_053025.4:c.2243C>G MANE Select	NP_444253.3:p.Pro748Arg
NM_053026.4:c.2036C>G	NP_444254.3:p.Pro679Arg
NM_053027.4:c.2243C>G	NP_444255.3:p.Pro748Arg
NM_053028.4:c.2036C>G	NP_444256.3:p.Pro679Arg