Canonical Allele Identifier: CA1591312107

Gene: GM2A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151259850C= , CM000667.2:g.151259850C=	GRCh38
NC_000005.9:g.150639411C= , CM000667.1:g.150639411C=	GRCh37
NC_000005.8:g.150619604C=	NCBI36
NG_009059.1:g.11799C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357164.4:c.177C= MANE Select	ENSP00000349687.3:p.Ile59=
ENST00000357164.3:c.177C=	ENSP00000349687.3:p.Ile59=
ENST00000523004.1:c.52C=
ENST00000523466.5:c.222C=	ENSP00000429100.1:p.Ile74=
NM_000405.4:c.177C=	NP_000396.2:p.Ile59=
NM_001167607.1:c.177C=	NP_001161079.1:p.Ile59=
NM_000405.5:c.177C= MANE Select	NP_000396.2:p.Ile59=
NM_001167607.2:c.177C=	NP_001161079.1:p.Ile59=
NM_001167607.3:c.177C=	NP_001161079.1:p.Ile59=