Canonical Allele Identifier: CA447179962

Gene: GM2A

Linked Data

• MyVariant Identifiers: chr5:g.150639471T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151259910T>G , CM000667.2:g.151259910T>G	GRCh38
NC_000005.9:g.150639471T>G , CM000667.1:g.150639471T>G	GRCh37
NC_000005.8:g.150619664T>G	NCBI36
NG_009059.1:g.11859T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357164.4:c.237T>G MANE Select	ENSP00000349687.3:p.Pro79=
ENST00000357164.3:c.237T>G	ENSP00000349687.3:p.Pro79=
ENST00000523004.1:c.112T>G
ENST00000523466.5:c.282T>G	ENSP00000429100.1:p.Pro94=
NM_000405.4:c.237T>G	NP_000396.2:p.Pro79=
NM_001167607.1:c.237T>G	NP_001161079.1:p.Pro79=
NM_000405.5:c.237T>G MANE Select	NP_000396.2:p.Pro79=
NM_001167607.2:c.237T>G	NP_001161079.1:p.Pro79=
NM_001167607.3:c.237T>G	NP_001161079.1:p.Pro79=