Canonical Allele Identifier: CA1591312142

Gene: GM2A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151259917G= , CM000667.2:g.151259917G=	GRCh38
NC_000005.9:g.150639478G= , CM000667.1:g.150639478G=	GRCh37
NC_000005.8:g.150619671G=	NCBI36
NG_009059.1:g.11866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357164.4:c.243+1G= MANE Select	ENSP00000349687.3:n.243+1G=
ENST00000357164.3:c.243+1G=	ENSP00000349687.3:n.243+1G=
ENST00000523004.1:c.118+1G=
ENST00000523466.5:c.288+1G=	ENSP00000429100.1:n.288+1G=
NM_000405.4:c.243+1G=	NP_000396.2:n.243+1G=
NM_001167607.1:c.243+1G=	NP_001161079.1:n.243+1G=
NM_000405.5:c.243+1G= MANE Select	NP_000396.2:n.243+1G=
NM_001167607.2:c.243+1G=	NP_001161079.1:n.243+1G=
NM_001167607.3:c.243+1G=	NP_001161079.1:n.243+1G=