Canonical Allele Identifier: CA2586548410

Gene: MYH14

Linked Data

• gnomAD v4: 19-50286318-GACACGGTTGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286321_50286331del , CM000681.2:g.50286321_50286331del	GRCh38
NC_000019.9:g.50789578_50789588del , CM000681.1:g.50789578_50789588del	GRCh37
NC_000019.8:g.55481390_55481400del	NCBI36
NG_011645.1:g.87694_87704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4441-161_4441-151del	ENSP00000407879.1:n.4441-161_4441-151del
ENST00000642316.2:c.4540-161_4540-151del MANE Select	ENSP00000493594.1:n.4540-161_4540-151del
ENST00000262269.12:c.1429-161_1429-151del	ENSP00000262269.9:n.1429-161_1429-151del
ENST00000376970.6:c.4417-161_4417-151del	ENSP00000366169.3:n.4417-161_4417-151del
ENST00000425460.5:c.4441-161_4441-151del	ENSP00000407879.1:n.4441-161_4441-151del
ENST00000440075.6:c.346-161_346-151del	ENSP00000406273.3:n.346-161_346-151del
ENST00000595016.1:n.1558_1568del
ENST00000596571.5:c.4417-161_4417-151del	ENSP00000472819.1:n.4417-161_4417-151del
ENST00000598205.5:c.4441-161_4441-151del	ENSP00000472543.1:n.4441-161_4441-151del
ENST00000601313.5:c.4540-161_4540-151del	ENSP00000470298.1:n.4540-161_4540-151del
NM_001077186.1:c.4441-161_4441-151del	NP_001070654.1:n.4441-161_4441-151del
NM_001145809.1:c.4540-161_4540-151del	NP_001139281.1:n.4540-161_4540-151del
NM_024729.3:c.4417-161_4417-151del	NP_079005.3:n.4417-161_4417-151del
XM_006723386.2:c.4441-161_4441-151del	XP_006723449.1:n.4441-161_4441-151del
XM_011527320.1:c.4561-161_4561-151del	XP_011525622.1:n.4561-161_4561-151del
XM_011527321.1:c.4537-161_4537-151del	XP_011525623.1:n.4537-161_4537-151del
XM_011527322.1:c.4465-161_4465-151del	XP_011525624.1:n.4465-161_4465-151del
XM_011527323.1:c.4441-161_4441-151del	XP_011525625.1:n.4441-161_4441-151del
XM_006723386.4:c.4441-161_4441-151del	XP_006723449.1:n.4441-161_4441-151del
XM_011527320.2:c.4561-161_4561-151del	XP_011525622.1:n.4561-161_4561-151del
XM_011527321.2:c.4537-161_4537-151del	XP_011525623.1:n.4537-161_4537-151del
XM_011527323.2:c.4441-161_4441-151del	XP_011525625.1:n.4441-161_4441-151del
XM_024451721.1:c.4417-161_4417-151del	XP_024307489.1:n.4417-161_4417-151del
NM_001077186.2:c.4441-161_4441-151del	NP_001070654.1:n.4441-161_4441-151del
NM_001145809.2:c.4540-161_4540-151del MANE Select	NP_001139281.1:n.4540-161_4540-151del
NM_024729.4:c.4417-161_4417-151del	NP_079005.3:n.4417-161_4417-151del