Canonical Allele Identifier: CA361805757

Gene: GM2A

Linked Data

• MyVariant Identifiers: chr5:g.150639334T>G (hg19) ; chr5:g.151259773T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151259773T>G , CM000667.2:g.151259773T>G	GRCh38
NC_000005.9:g.150639334T>G , CM000667.1:g.150639334T>G	GRCh37
NC_000005.8:g.150619527T>G	NCBI36
NG_009059.1:g.11722T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357164.4:c.100T>G MANE Select	ENSP00000349687.3:p.Phe34Val
ENST00000357164.3:c.100T>G	ENSP00000349687.3:p.Phe34Val
ENST00000523466.5:c.145T>G	ENSP00000429100.1:p.Phe49Val
NM_000405.4:c.100T>G	NP_000396.2:p.Phe34Val
NM_001167607.1:c.100T>G	NP_001161079.1:p.Phe34Val
NM_000405.5:c.100T>G MANE Select	NP_000396.2:p.Phe34Val
NM_001167607.2:c.100T>G	NP_001161079.1:p.Phe34Val
NM_001167607.3:c.100T>G	NP_001161079.1:p.Phe34Val