Canonical Allele Identifier: CA386304929

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179865C>A (hg19) ; chr12:g.101786087C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786087C>A , CM000674.2:g.101786087C>A	GRCh38
NC_000012.11:g.102179865C>A , CM000674.1:g.102179865C>A	GRCh37
NC_000012.10:g.100703996C>A	NCBI36
NG_021243.1:g.49781G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.496G>T MANE Select	ENSP00000299314.7:p.Asp166Tyr
ENST00000299314.11:c.496G>T	ENSP00000299314.7:p.Asp166Tyr
ENST00000549940.5:c.496G>T	ENSP00000449150.1:p.Asp166Tyr
ENST00000550352.1:n.290G>T
ENST00000552681.1:c.130G>T	ENSP00000449217.1:p.Asp44Tyr
NM_024312.4:c.496G>T	NP_077288.2:p.Asp166Tyr
XM_006719593.2:c.496G>T	XP_006719656.1:p.Asp166Tyr
XM_011538731.1:c.415G>T	XP_011537033.1:p.Asp139Tyr
XM_006719593.3:c.496G>T	XP_006719656.1:p.Asp166Tyr
XM_011538731.2:c.415G>T	XP_011537033.1:p.Asp139Tyr
XM_017019961.1:c.280G>T	XP_016875450.1:p.Asp94Tyr
XM_017019962.2:c.-855G>T	XP_016875451.1:n.-855G>T
NM_024312.5:c.496G>T MANE Select	NP_077288.2:p.Asp166Tyr