Canonical Allele Identifier: CA2340793470

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50217817G= , CM000681.2:g.50217817G=	GRCh38
NC_000019.9:g.50721074G= , CM000681.1:g.50721074G=	GRCh37
NC_000019.8:g.55412886G=	NCBI36
NG_011645.1:g.19190G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001145809.2:c.562+46G= MANE Select	NP_001139281.1:n.562+46G=
ENST00000642316.2:c.562+46G= MANE Select	ENSP00000493594.1:n.562+46G=
NM_001077186.1:c.562+46G=	NP_001070654.1:n.562+46G=
NM_001077186.2:c.562+46G=	NP_001070654.1:n.562+46G=
NM_001145809.1:c.562+46G=	NP_001139281.1:n.562+46G=
NM_024729.3:c.562+46G=	NP_079005.3:n.562+46G=
NM_024729.4:c.562+46G=	NP_079005.3:n.562+46G=
ENST00000376970.6:c.562+46G=	ENSP00000366169.3:n.562+46G=
ENST00000425460.5:c.562+46G=	ENSP00000407879.1:n.562+46G=
ENST00000425460.6:c.562+46G=	ENSP00000407879.1:n.562+46G=
ENST00000440075.6:c.-1729+46G=	ENSP00000406273.3:n.-1729+46G=
ENST00000596571.5:c.562+46G=	ENSP00000472819.1:n.562+46G=
ENST00000598205.5:c.562+46G=	ENSP00000472543.1:n.562+46G=
ENST00000599920.5:c.562+46G=	ENSP00000469573.1:n.562+46G=
ENST00000601313.5:c.562+46G=	ENSP00000470298.1:n.562+46G=
ENST00000646861.1:c.562+46G=	ENSP00000493667.1:n.562+46G=
XM_006723386.2:c.562+46G=	XP_006723449.1:n.562+46G=
XM_006723386.4:c.562+46G=	XP_006723449.1:n.562+46G=
XM_011527320.1:c.682+46G=	XP_011525622.1:n.682+46G=
XM_011527320.2:c.682+46G=	XP_011525622.1:n.682+46G=
XM_011527321.1:c.682+46G=	XP_011525623.1:n.682+46G=
XM_011527321.2:c.682+46G=	XP_011525623.1:n.682+46G=
XM_011527322.1:c.682+46G=	XP_011525624.1:n.682+46G=
XM_011527323.1:c.562+46G=	XP_011525625.1:n.562+46G=
XM_011527323.2:c.562+46G=	XP_011525625.1:n.562+46G=
XM_024451721.1:c.562+46G=	XP_024307489.1:n.562+46G=