Canonical Allele Identifier: CA2340825445

Gene: MYH14

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286373_50286383delinsGTCTCTTTCTC , CM000681.2:g.50286373_50286383delinsGTCTCTTTCTC	GRCh38
NC_000019.9:g.50789630_50789640delinsGTCTCTTTCTC , CM000681.1:g.50789630_50789640delinsGTCTCTTTCTC	GRCh37
NC_000019.8:g.55481442_55481452delinsGTCTCTTTCTC	NCBI36
NG_011645.1:g.87746_87756delinsGTCTCTTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4441-109_4441-99delinsGTCTCTTTCTC	ENSP00000407879.1:n.4441-109_4441-99delinsGTCTCTTTCTC
ENST00000642316.2:c.4540-109_4540-99delinsGTCTCTTTCTC MANE Select	ENSP00000493594.1:n.4540-109_4540-99delinsGTCTCTTTCTC
ENST00000262269.12:c.1429-109_1429-99delinsGTCTCTTTCTC	ENSP00000262269.9:n.1429-109_1429-99delinsGTCTCTTTCTC
ENST00000376970.6:c.4417-109_4417-99delinsGTCTCTTTCTC	ENSP00000366169.3:n.4417-109_4417-99delinsGTCTCTTTCTC
ENST00000425460.5:c.4441-109_4441-99delinsGTCTCTTTCTC	ENSP00000407879.1:n.4441-109_4441-99delinsGTCTCTTTCTC
ENST00000440075.6:c.346-109_346-99delinsGTCTCTTTCTC	ENSP00000406273.3:n.346-109_346-99delinsGTCTCTTTCTC
ENST00000595016.1:n.1610_1620delinsGTCTCTTTCTC
ENST00000596571.5:c.4417-109_4417-99delinsGTCTCTTTCTC	ENSP00000472819.1:n.4417-109_4417-99delinsGTCTCTTTCTC
ENST00000598205.5:c.4441-109_4441-99delinsGTCTCTTTCTC	ENSP00000472543.1:n.4441-109_4441-99delinsGTCTCTTTCTC
ENST00000601313.5:c.4540-109_4540-99delinsGTCTCTTTCTC	ENSP00000470298.1:n.4540-109_4540-99delinsGTCTCTTTCTC
NM_001077186.1:c.4441-109_4441-99delinsGTCTCTTTCTC	NP_001070654.1:n.4441-109_4441-99delinsGTCTCTTTCTC
NM_001145809.1:c.4540-109_4540-99delinsGTCTCTTTCTC	NP_001139281.1:n.4540-109_4540-99delinsGTCTCTTTCTC
NM_024729.3:c.4417-109_4417-99delinsGTCTCTTTCTC	NP_079005.3:n.4417-109_4417-99delinsGTCTCTTTCTC
XM_006723386.2:c.4441-109_4441-99delinsGTCTCTTTCTC	XP_006723449.1:n.4441-109_4441-99delinsGTCTCTTTCTC
XM_011527320.1:c.4561-109_4561-99delinsGTCTCTTTCTC	XP_011525622.1:n.4561-109_4561-99delinsGTCTCTTTCTC
XM_011527321.1:c.4537-109_4537-99delinsGTCTCTTTCTC	XP_011525623.1:n.4537-109_4537-99delinsGTCTCTTTCTC
XM_011527322.1:c.4465-109_4465-99delinsGTCTCTTTCTC	XP_011525624.1:n.4465-109_4465-99delinsGTCTCTTTCTC
XM_011527323.1:c.4441-109_4441-99delinsGTCTCTTTCTC	XP_011525625.1:n.4441-109_4441-99delinsGTCTCTTTCTC
XM_006723386.4:c.4441-109_4441-99delinsGTCTCTTTCTC	XP_006723449.1:n.4441-109_4441-99delinsGTCTCTTTCTC
XM_011527320.2:c.4561-109_4561-99delinsGTCTCTTTCTC	XP_011525622.1:n.4561-109_4561-99delinsGTCTCTTTCTC
XM_011527321.2:c.4537-109_4537-99delinsGTCTCTTTCTC	XP_011525623.1:n.4537-109_4537-99delinsGTCTCTTTCTC
XM_011527323.2:c.4441-109_4441-99delinsGTCTCTTTCTC	XP_011525625.1:n.4441-109_4441-99delinsGTCTCTTTCTC
XM_024451721.1:c.4417-109_4417-99delinsGTCTCTTTCTC	XP_024307489.1:n.4417-109_4417-99delinsGTCTCTTTCTC
NM_001077186.2:c.4441-109_4441-99delinsGTCTCTTTCTC	NP_001070654.1:n.4441-109_4441-99delinsGTCTCTTTCTC
NM_001145809.2:c.4540-109_4540-99delinsGTCTCTTTCTC MANE Select	NP_001139281.1:n.4540-109_4540-99delinsGTCTCTTTCTC
NM_024729.4:c.4417-109_4417-99delinsGTCTCTTTCTC	NP_079005.3:n.4417-109_4417-99delinsGTCTCTTTCTC