Canonical Allele Identifier: CA386296206

Gene: GNPTAB

Linked Data

• dbSNP Id: rs1443484087
• MyVariant Identifiers: chr12:g.102155402T>C (hg19) ; chr12:g.101761624T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761624T>C , CM000674.2:g.101761624T>C	GRCh38
NC_000012.11:g.102155402T>C , CM000674.1:g.102155402T>C	GRCh37
NC_000012.10:g.100679533T>C	NCBI36
NG_021243.1:g.74244A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2855A>G MANE Select	ENSP00000299314.7:p.Lys952Arg
ENST00000299314.11:c.2855A>G	ENSP00000299314.7:p.Lys952Arg
NM_024312.4:c.2855A>G	NP_077288.2:p.Lys952Arg
XM_006719593.2:c.2855A>G	XP_006719656.1:p.Lys952Arg
XM_011538731.1:c.2774A>G	XP_011537033.1:p.Lys925Arg
XM_006719593.3:c.2855A>G	XP_006719656.1:p.Lys952Arg
XM_011538731.2:c.2774A>G	XP_011537033.1:p.Lys925Arg
XM_017019961.1:c.2639A>G	XP_016875450.1:p.Lys880Arg
XM_017019962.2:c.1628A>G	XP_016875451.1:p.Lys543Arg
NM_024312.5:c.2855A>G MANE Select	NP_077288.2:p.Lys952Arg