Canonical Allele Identifier: CA2739279722

Gene: MYLK

Linked Data

• ClinVar Variation Id: 2898386
• ClinVar RCV Id: RCV003642034

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123708012T>G , CM000665.2:g.123708012T>G	GRCh38
NC_000003.11:g.123426859T>G , CM000665.1:g.123426859T>G	GRCh37
NC_000003.10:g.124909549T>G	NCBI36
NG_029111.1:g.181291A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.1934-9A>C	ENSP00000320622.6:n.1934-9A>C
ENST00000686406.1:c.2141-9A>C	ENSP00000509044.1:n.2141-9A>C
ENST00000686761.1:c.2141-9A>C	ENSP00000508758.1:n.2141-9A>C
ENST00000686822.1:n.2035-9A>C
ENST00000687848.1:c.2171-9A>C	ENSP00000508761.1:n.2171-9A>C
ENST00000690457.1:c.1379-9A>C	ENSP00000508777.1:n.1379-9A>C
ENST00000693689.1:c.1934-9A>C	ENSP00000510503.1:n.1934-9A>C
ENST00000360304.8:c.2141-9A>C MANE Select	ENSP00000353452.3:n.2141-9A>C
ENST00000346322.9:c.1934-9A>C	ENSP00000320622.5:n.1934-9A>C
ENST00000354792.9:c.1934-9A>C	ENSP00000346846.6:n.1934-9A>C
ENST00000359169.5:c.2141-9A>C	ENSP00000352088.1:n.2141-9A>C
ENST00000360304.7:c.2141-9A>C	ENSP00000353452.3:n.2141-9A>C
ENST00000360772.7:c.2141-9A>C	ENSP00000354004.3:n.2141-9A>C
ENST00000464489.5:c.*1720-9A>C	ENSP00000417798.1:n.*1720-9A>C
ENST00000475616.5:c.2141-9A>C	ENSP00000418335.1:n.2141-9A>C
NM_053025.3:c.2141-9A>C	NP_444253.3:n.2141-9A>C
NM_053026.3:c.1934-9A>C	NP_444254.3:n.1934-9A>C
NM_053027.3:c.2141-9A>C	NP_444255.3:n.2141-9A>C
NM_053028.3:c.1934-9A>C	NP_444256.3:n.1934-9A>C
XM_011512860.1:c.2141-9A>C	XP_011511162.1:n.2141-9A>C
XM_011512861.1:c.2141-9A>C	XP_011511163.1:n.2141-9A>C
XM_011512862.1:c.1613-9A>C	XP_011511164.1:n.1613-9A>C
XR_241556.2:n.313+4003T>G
XR_427403.2:n.406+4003T>G
XR_924414.1:n.406+4003T>G
XR_924415.1:n.403+4003T>G
XR_924416.1:n.230+4003T>G
XR_924417.1:n.226+4003T>G
XR_924418.1:n.406+4003T>G
NM_001321309.1:c.1613-9A>C	NP_001308238.1:n.1613-9A>C
XM_011512860.3:c.2171-9A>C	XP_011511162.2:n.2171-9A>C
XM_011512861.3:c.2171-9A>C	XP_011511163.2:n.2171-9A>C
XM_024453532.1:c.2171-9A>C	XP_024309300.1:n.2171-9A>C
XM_024453533.1:c.2141-9A>C	XP_024309301.1:n.2141-9A>C
XM_024453534.1:c.1964-9A>C	XP_024309302.1:n.1964-9A>C
XM_024453535.1:c.1934-9A>C	XP_024309303.1:n.1934-9A>C
XM_024453536.1:c.2141-9A>C	XP_024309304.1:n.2141-9A>C
XM_024453537.1:c.2141-9A>C	XP_024309305.1:n.2141-9A>C
XR_001740871.2:n.406+4003T>G
XR_427403.4:n.406+4003T>G
XR_924414.3:n.406+4003T>G
XR_924417.3:n.251+4003T>G
XR_924418.3:n.406+4003T>G
NM_001321309.2:c.1613-9A>C	NP_001308238.1:n.1613-9A>C
NM_053025.4:c.2141-9A>C MANE Select	NP_444253.3:n.2141-9A>C
NM_053026.4:c.1934-9A>C	NP_444254.3:n.1934-9A>C
NM_053027.4:c.2141-9A>C	NP_444255.3:n.2141-9A>C
NM_053028.4:c.1934-9A>C	NP_444256.3:n.1934-9A>C