Canonical Allele Identifier: CA386294820

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153884G>T (hg19) ; chr12:g.101760106G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760106G>T , CM000674.2:g.101760106G>T	GRCh38
NC_000012.11:g.102153884G>T , CM000674.1:g.102153884G>T	GRCh37
NC_000012.10:g.100678015G>T	NCBI36
NG_021243.1:g.75762C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3173C>A MANE Select	ENSP00000299314.7:p.Ser1058Ter
ENST00000299314.11:c.3173C>A	ENSP00000299314.7:p.Ser1058Ter
ENST00000549194.1:n.39C>A
NM_024312.4:c.3173C>A	NP_077288.2:p.Ser1058Ter
XM_006719593.2:c.3173C>A	XP_006719656.1:p.Ser1058Ter
XM_011538731.1:c.3092C>A	XP_011537033.1:p.Ser1031Ter
XM_006719593.3:c.3173C>A	XP_006719656.1:p.Ser1058Ter
XM_011538731.2:c.3092C>A	XP_011537033.1:p.Ser1031Ter
XM_017019961.1:c.2957C>A	XP_016875450.1:p.Ser986Ter
XM_017019962.2:c.1946C>A	XP_016875451.1:p.Ser649Ter
NM_024312.5:c.3173C>A MANE Select	NP_077288.2:p.Ser1058Ter