Canonical Allele Identifier: CA447179859

Gene: GM2A

Linked Data

• MyVariant Identifiers: chr5:g.150639378C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151259817C>T , CM000667.2:g.151259817C>T	GRCh38
NC_000005.9:g.150639378C>T , CM000667.1:g.150639378C>T	GRCh37
NC_000005.8:g.150619571C>T	NCBI36
NG_009059.1:g.11766C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357164.4:c.144C>T MANE Select	ENSP00000349687.3:p.Ile48=
ENST00000357164.3:c.144C>T	ENSP00000349687.3:p.Ile48=
ENST00000523004.1:c.19C>T
ENST00000523466.5:c.189C>T	ENSP00000429100.1:p.Ile63=
NM_000405.4:c.144C>T	NP_000396.2:p.Ile48=
NM_001167607.1:c.144C>T	NP_001161079.1:p.Ile48=
NM_000405.5:c.144C>T MANE Select	NP_000396.2:p.Ile48=
NM_001167607.2:c.144C>T	NP_001161079.1:p.Ile48=
NM_001167607.3:c.144C>T	NP_001161079.1:p.Ile48=