Canonical Allele Identifier: CA386304964

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179880A>C (hg19) ; chr12:g.101786102A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786102A>C , CM000674.2:g.101786102A>C	GRCh38
NC_000012.11:g.102179880A>C , CM000674.1:g.102179880A>C	GRCh37
NC_000012.10:g.100704011A>C	NCBI36
NG_021243.1:g.49766T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.481T>G MANE Select	ENSP00000299314.7:p.Phe161Val
ENST00000299314.11:c.481T>G	ENSP00000299314.7:p.Phe161Val
ENST00000549940.5:c.481T>G	ENSP00000449150.1:p.Phe161Val
ENST00000550352.1:n.275T>G
ENST00000552681.1:c.115T>G	ENSP00000449217.1:p.Phe39Val
NM_024312.4:c.481T>G	NP_077288.2:p.Phe161Val
XM_006719593.2:c.481T>G	XP_006719656.1:p.Phe161Val
XM_011538731.1:c.400T>G	XP_011537033.1:p.Phe134Val
XM_006719593.3:c.481T>G	XP_006719656.1:p.Phe161Val
XM_011538731.2:c.400T>G	XP_011537033.1:p.Phe134Val
XM_017019961.1:c.265T>G	XP_016875450.1:p.Phe89Val
XM_017019962.2:c.-870T>G	XP_016875451.1:n.-870T>G
NM_024312.5:c.481T>G MANE Select	NP_077288.2:p.Phe161Val