Canonical Allele Identifier: CA6746611

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101766281C>T , CM000674.2:g.101766281C>T	GRCh38
NC_000012.11:g.102160059C>T , CM000674.1:g.102160059C>T	GRCh37
NC_000012.10:g.100684190C>T	NCBI36
NG_021243.1:g.69587G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024312.5:c.1422G>A MANE Select	NP_077288.2:p.Gly474=
ENST00000299314.12:c.1422G>A MANE Select	ENSP00000299314.7:p.Gly474=
NM_024312.4:c.1422G>A	NP_077288.2:p.Gly474=
ENST00000299314.11:c.1422G>A	ENSP00000299314.7:p.Gly474=
ENST00000552009.1:n.81G>A
XM_006719593.2:c.1422G>A	XP_006719656.1:p.Gly474=
XM_006719593.3:c.1422G>A	XP_006719656.1:p.Gly474=
XM_011538731.1:c.1341G>A	XP_011537033.1:p.Gly447=
XM_011538731.2:c.1341G>A	XP_011537033.1:p.Gly447=
XM_017019961.1:c.1206G>A	XP_016875450.1:p.Gly402=
XM_017019962.2:c.195G>A	XP_016875451.1:p.Gly65=