Canonical Allele Identifier: CA2247222233

Gene: MYH8 MYHAS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10409165_10409167delinsCTG , CM000679.2:g.10409165_10409167delinsCTG	GRCh38
NC_000017.10:g.10312482_10312484delinsCTG , CM000679.1:g.10312482_10312484delinsCTG	GRCh37
NC_000017.9:g.10253207_10253209delinsCTG	NCBI36
NG_013015.1:g.17784_17786delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403437.2:c.1898-3_1898-1delinsCAG (MYH8) MANE Select	ENSP00000384330.2:n.1898-3_1898-1delinsCAG
NM_002472.2:c.1898-3_1898-1delinsCAG (MYH8)	NP_002463.2:n.1898-3_1898-1delinsCAG
NR_125367.1:n.167+2927_167+2929delinsCTG (MYHAS)
XM_011523873.1:c.1898-3_1898-1delinsCAG (MYH8)	XP_011522175.1:n.1898-3_1898-1delinsCAG
XM_011523874.1:c.1898-3_1898-1delinsCAG (MYH8)	XP_011522176.1:n.1898-3_1898-1delinsCAG
NM_002472.3:c.1898-3_1898-1delinsCAG (MYH8) MANE Select	NP_002463.2:n.1898-3_1898-1delinsCAG