Canonical Allele Identifier: CA386301886

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102161855A>T (hg19) ; chr12:g.101768077A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101768077A>T , CM000674.2:g.101768077A>T	GRCh38
NC_000012.11:g.102161855A>T , CM000674.1:g.102161855A>T	GRCh37
NC_000012.10:g.100685986A>T	NCBI36
NG_021243.1:g.67791T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1368T>A MANE Select	ENSP00000299314.7:p.Cys456Ter
ENST00000299314.11:c.1368T>A	ENSP00000299314.7:p.Cys456Ter
ENST00000549940.5:c.1368T>A	ENSP00000449150.1:p.Cys456Ter
ENST00000552009.1:n.27T>A
NM_024312.4:c.1368T>A	NP_077288.2:p.Cys456Ter
XM_006719593.2:c.1368T>A	XP_006719656.1:p.Cys456Ter
XM_011538731.1:c.1287T>A	XP_011537033.1:p.Cys429Ter
XM_006719593.3:c.1368T>A	XP_006719656.1:p.Cys456Ter
XM_011538731.2:c.1287T>A	XP_011537033.1:p.Cys429Ter
XM_017019961.1:c.1152T>A	XP_016875450.1:p.Cys384Ter
XM_017019962.2:c.141T>A	XP_016875451.1:p.Cys47Ter
NM_024312.5:c.1368T>A MANE Select	NP_077288.2:p.Cys456Ter