Canonical Allele Identifier: CA633896818

Gene: MYH14

Linked Data

• dbSNP Id: rs1378802662
• gnomAD v2: 19-50789663-CT-C
• gnomAD v3: 19-50286406-CT-C
• gnomAD v4: 19-50286406-CT-C
• MyVariant Identifiers: chr19:g.50789664del (hg19) ; chr19:g.50286407del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50286407del , CM000681.2:g.50286407del	GRCh38
NC_000019.9:g.50789664del , CM000681.1:g.50789664del	GRCh37
NC_000019.8:g.55481476del	NCBI36
NG_011645.1:g.87780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425460.6:c.4441-75del	ENSP00000407879.1:n.4441-75del
ENST00000642316.2:c.4540-75del MANE Select	ENSP00000493594.1:n.4540-75del
ENST00000262269.12:c.1429-75del	ENSP00000262269.9:n.1429-75del
ENST00000376970.6:c.4417-75del	ENSP00000366169.3:n.4417-75del
ENST00000425460.5:c.4441-75del	ENSP00000407879.1:n.4441-75del
ENST00000440075.6:c.346-75del	ENSP00000406273.3:n.346-75del
ENST00000595016.1:n.1644del
ENST00000596571.5:c.4417-75del	ENSP00000472819.1:n.4417-75del
ENST00000598205.5:c.4441-75del	ENSP00000472543.1:n.4441-75del
ENST00000601313.5:c.4540-75del	ENSP00000470298.1:n.4540-75del
NM_001077186.1:c.4441-75del	NP_001070654.1:n.4441-75del
NM_001145809.1:c.4540-75del	NP_001139281.1:n.4540-75del
NM_024729.3:c.4417-75del	NP_079005.3:n.4417-75del
XM_006723386.2:c.4441-75del	XP_006723449.1:n.4441-75del
XM_011527320.1:c.4561-75del	XP_011525622.1:n.4561-75del
XM_011527321.1:c.4537-75del	XP_011525623.1:n.4537-75del
XM_011527322.1:c.4465-75del	XP_011525624.1:n.4465-75del
XM_011527323.1:c.4441-75del	XP_011525625.1:n.4441-75del
XM_006723386.4:c.4441-75del	XP_006723449.1:n.4441-75del
XM_011527320.2:c.4561-75del	XP_011525622.1:n.4561-75del
XM_011527321.2:c.4537-75del	XP_011525623.1:n.4537-75del
XM_011527323.2:c.4441-75del	XP_011525625.1:n.4441-75del
XM_024451721.1:c.4417-75del	XP_024307489.1:n.4417-75del
NM_001077186.2:c.4441-75del	NP_001070654.1:n.4441-75del
NM_001145809.2:c.4540-75del MANE Select	NP_001139281.1:n.4540-75del
NM_024729.4:c.4417-75del	NP_079005.3:n.4417-75del