Canonical Allele Identifier: CA2586545546

Gene: MYH14

Linked Data

• gnomAD v4: 19-50268332-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50268335del , CM000681.2:g.50268335del	GRCh38
NC_000019.9:g.50771592del , CM000681.1:g.50771592del	GRCh37
NC_000019.8:g.55463404del	NCBI36
NG_011645.1:g.69708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.2902del	ENSP00000407879.1:p.Thr968ProfsTer13
ENST00000642316.2:c.3001del MANE Select	ENSP00000493594.1:p.Thr1001ProfsTer13
ENST00000376970.6:c.2878del	ENSP00000366169.3:p.Thr960ProfsTer13
ENST00000425460.5:c.2902del	ENSP00000407879.1:p.Thr968ProfsTer13
ENST00000440075.6:c.-727-7656del	ENSP00000406273.3:n.-727-7656del
ENST00000596571.5:c.2878del	ENSP00000472819.1:p.Thr960ProfsTer13
ENST00000598205.5:c.2902del	ENSP00000472543.1:p.Thr968ProfsTer13
ENST00000599920.5:c.2902del	ENSP00000469573.1:p.Thr968ProfsTer13
ENST00000601313.5:c.3001del	ENSP00000470298.1:p.Thr1001ProfsTer13
NM_001077186.1:c.2902del	NP_001070654.1:p.Thr968ProfsTer13
NM_001145809.1:c.3001del	NP_001139281.1:p.Thr1001ProfsTer13
NM_024729.3:c.2878del	NP_079005.3:p.Thr960ProfsTer13
XM_006723386.2:c.2902del	XP_006723449.1:p.Thr968ProfsTer13
XM_011527320.1:c.3022del	XP_011525622.1:p.Thr1008ProfsTer13
XM_011527321.1:c.2998del	XP_011525623.1:p.Thr1000ProfsTer13
XM_011527322.1:c.2926del	XP_011525624.1:p.Thr976ProfsTer13
XM_011527323.1:c.2902del	XP_011525625.1:p.Thr968ProfsTer13
XM_006723386.4:c.2902del	XP_006723449.1:p.Thr968ProfsTer13
XM_011527320.2:c.3022del	XP_011525622.1:p.Thr1008ProfsTer13
XM_011527321.2:c.2998del	XP_011525623.1:p.Thr1000ProfsTer13
XM_011527323.2:c.2902del	XP_011525625.1:p.Thr968ProfsTer13
XM_024451721.1:c.2878del	XP_024307489.1:p.Thr960ProfsTer13
NM_001077186.2:c.2902del	NP_001070654.1:p.Thr968ProfsTer13
NM_001145809.2:c.3001del MANE Select	NP_001139281.1:p.Thr1001ProfsTer13
NM_024729.4:c.2878del	NP_079005.3:p.Thr960ProfsTer13