Canonical Allele Identifier: CA481577255

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102164205T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770427T>A , CM000674.2:g.101770427T>A	GRCh38
NC_000012.11:g.102164205T>A , CM000674.1:g.102164205T>A	GRCh37
NC_000012.10:g.100688336T>A	NCBI36
NG_021243.1:g.65441A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1092A>T MANE Select	ENSP00000299314.7:p.Arg364=
ENST00000299314.11:c.1092A>T	ENSP00000299314.7:p.Arg364=
ENST00000549940.5:c.1092A>T	ENSP00000449150.1:p.Arg364=
NM_024312.4:c.1092A>T	NP_077288.2:p.Arg364=
XM_006719593.2:c.1092A>T	XP_006719656.1:p.Arg364=
XM_011538731.1:c.1011A>T	XP_011537033.1:p.Arg337=
XM_006719593.3:c.1092A>T	XP_006719656.1:p.Arg364=
XM_011538731.2:c.1011A>T	XP_011537033.1:p.Arg337=
XM_017019961.1:c.876A>T	XP_016875450.1:p.Arg292=
XM_017019962.2:c.-136A>T	XP_016875451.1:n.-136A>T
NM_024312.5:c.1092A>T MANE Select	NP_077288.2:p.Arg364=