Canonical Allele Identifier: CA2586548445

Gene: MYH14

Linked Data

• gnomAD v4: 19-50286353-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286353T>C , CM000681.2:g.50286353T>C	GRCh38
NC_000019.9:g.50789610T>C , CM000681.1:g.50789610T>C	GRCh37
NC_000019.8:g.55481422T>C	NCBI36
NG_011645.1:g.87726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4441-129T>C	ENSP00000407879.1:n.4441-129T>C
ENST00000642316.2:c.4540-129T>C MANE Select	ENSP00000493594.1:n.4540-129T>C
ENST00000262269.12:c.1429-129T>C	ENSP00000262269.9:n.1429-129T>C
ENST00000376970.6:c.4417-129T>C	ENSP00000366169.3:n.4417-129T>C
ENST00000425460.5:c.4441-129T>C	ENSP00000407879.1:n.4441-129T>C
ENST00000440075.6:c.346-129T>C	ENSP00000406273.3:n.346-129T>C
ENST00000595016.1:n.1590T>C
ENST00000596571.5:c.4417-129T>C	ENSP00000472819.1:n.4417-129T>C
ENST00000598205.5:c.4441-129T>C	ENSP00000472543.1:n.4441-129T>C
ENST00000601313.5:c.4540-129T>C	ENSP00000470298.1:n.4540-129T>C
NM_001077186.1:c.4441-129T>C	NP_001070654.1:n.4441-129T>C
NM_001145809.1:c.4540-129T>C	NP_001139281.1:n.4540-129T>C
NM_024729.3:c.4417-129T>C	NP_079005.3:n.4417-129T>C
XM_006723386.2:c.4441-129T>C	XP_006723449.1:n.4441-129T>C
XM_011527320.1:c.4561-129T>C	XP_011525622.1:n.4561-129T>C
XM_011527321.1:c.4537-129T>C	XP_011525623.1:n.4537-129T>C
XM_011527322.1:c.4465-129T>C	XP_011525624.1:n.4465-129T>C
XM_011527323.1:c.4441-129T>C	XP_011525625.1:n.4441-129T>C
XM_006723386.4:c.4441-129T>C	XP_006723449.1:n.4441-129T>C
XM_011527320.2:c.4561-129T>C	XP_011525622.1:n.4561-129T>C
XM_011527321.2:c.4537-129T>C	XP_011525623.1:n.4537-129T>C
XM_011527323.2:c.4441-129T>C	XP_011525625.1:n.4441-129T>C
XM_024451721.1:c.4417-129T>C	XP_024307489.1:n.4417-129T>C
NM_001077186.2:c.4441-129T>C	NP_001070654.1:n.4441-129T>C
NM_001145809.2:c.4540-129T>C MANE Select	NP_001139281.1:n.4540-129T>C
NM_024729.4:c.4417-129T>C	NP_079005.3:n.4417-129T>C