Canonical Allele Identifier: CA400022602

Gene: MYL4

Linked Data

• MyVariant Identifiers: chr17:g.45299183T>C (hg19) ; chr17:g.47221817T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221817T>C , CM000679.2:g.47221817T>C	GRCh38
NC_000017.10:g.45299183T>C , CM000679.1:g.45299183T>C	GRCh37
NC_000017.9:g.42654182T>C	NCBI36
NG_052847.1:g.17801T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.449T>C	ENSP00000347055.1:p.Val150Ala
ENST00000393450.5:c.449T>C MANE Select	ENSP00000377096.1:p.Val150Ala
ENST00000536623.6:c.449T>C	ENSP00000442375.2:p.Val150Ala
ENST00000570671.1:c.160T>C
ENST00000570772.5:c.*235T>C	ENSP00000458194.1:n.*235T>C
ENST00000571981.5:c.*235T>C	ENSP00000459035.1:n.*235T>C
ENST00000572316.5:c.449T>C	ENSP00000461570.1:p.Val150Ala
ENST00000573747.6:c.*51T>C	ENSP00000460734.1:n.*51T>C
ENST00000576874.5:c.449T>C	ENSP00000458907.1:p.Val150Ala
NM_001002841.1:c.449T>C	NP_001002841.1:p.Val150Ala
NM_002476.2:c.449T>C MANE Select	NP_002467.1:p.Val150Ala
XM_005257391.3:c.449T>C	XP_005257448.1:p.Val150Ala
XM_011524838.1:c.449T>C	XP_011523140.1:p.Val150Ala
XM_011524839.1:c.239T>C	XP_011523141.1:p.Val80Ala
XM_005257391.5:c.449T>C	XP_005257448.1:p.Val150Ala
XM_011524839.2:c.542T>C	XP_011523141.2:p.Val181Ala
XM_017024683.1:c.542T>C	XP_016880172.1:p.Val181Ala
XM_024450766.1:c.542T>C	XP_024306534.1:p.Val181Ala
NM_001002841.2:c.449T>C	NP_001002841.1:p.Val150Ala