Canonical Allele Identifier: CA386304898

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179852A>C (hg19) ; chr12:g.101786074A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786074A>C , CM000674.2:g.101786074A>C	GRCh38
NC_000012.11:g.102179852A>C , CM000674.1:g.102179852A>C	GRCh37
NC_000012.10:g.100703983A>C	NCBI36
NG_021243.1:g.49794T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.509T>G MANE Select	ENSP00000299314.7:p.Val170Gly
ENST00000299314.11:c.509T>G	ENSP00000299314.7:p.Val170Gly
ENST00000549940.5:c.509T>G	ENSP00000449150.1:p.Val170Gly
ENST00000550352.1:n.303T>G
ENST00000552681.1:c.143T>G	ENSP00000449217.1:p.Val48Gly
NM_024312.4:c.509T>G	NP_077288.2:p.Val170Gly
XM_006719593.2:c.509T>G	XP_006719656.1:p.Val170Gly
XM_011538731.1:c.428T>G	XP_011537033.1:p.Val143Gly
XM_006719593.3:c.509T>G	XP_006719656.1:p.Val170Gly
XM_011538731.2:c.428T>G	XP_011537033.1:p.Val143Gly
XM_017019961.1:c.293T>G	XP_016875450.1:p.Val98Gly
XM_017019962.2:c.-842T>G	XP_016875451.1:n.-842T>G
NM_024312.5:c.509T>G MANE Select	NP_077288.2:p.Val170Gly