Canonical Allele Identifier: CA386296386

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155482C>A (hg19) ; chr12:g.101761704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761704C>A , CM000674.2:g.101761704C>A	GRCh38
NC_000012.11:g.102155482C>A , CM000674.1:g.102155482C>A	GRCh37
NC_000012.10:g.100679613C>A	NCBI36
NG_021243.1:g.74164G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2775G>T MANE Select	ENSP00000299314.7:p.Arg925Ser
ENST00000299314.11:c.2775G>T	ENSP00000299314.7:p.Arg925Ser
NM_024312.4:c.2775G>T	NP_077288.2:p.Arg925Ser
XM_006719593.2:c.2775G>T	XP_006719656.1:p.Arg925Ser
XM_011538731.1:c.2694G>T	XP_011537033.1:p.Arg898Ser
XM_006719593.3:c.2775G>T	XP_006719656.1:p.Arg925Ser
XM_011538731.2:c.2694G>T	XP_011537033.1:p.Arg898Ser
XM_017019961.1:c.2559G>T	XP_016875450.1:p.Arg853Ser
XM_017019962.2:c.1548G>T	XP_016875451.1:p.Arg516Ser
NM_024312.5:c.2775G>T MANE Select	NP_077288.2:p.Arg925Ser