Canonical Allele Identifier: CA386298316

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101764513G>A , CM000674.2:g.101764513G>A	GRCh38
NC_000012.11:g.102158291G>A , CM000674.1:g.102158291G>A	GRCh37
NC_000012.10:g.100682422G>A	NCBI36
NG_021243.1:g.71355C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024312.5:c.2404C>T MANE Select	NP_077288.2:p.Gln802Ter
ENST00000299314.12:c.2404C>T MANE Select	ENSP00000299314.7:p.Gln802Ter
NM_024312.4:c.2404C>T	NP_077288.2:p.Gln802Ter
ENST00000299314.11:c.2404C>T	ENSP00000299314.7:p.Gln802Ter
XM_006719593.2:c.2404C>T	XP_006719656.1:p.Gln802Ter
XM_006719593.3:c.2404C>T	XP_006719656.1:p.Gln802Ter
XM_011538731.1:c.2323C>T	XP_011537033.1:p.Gln775Ter
XM_011538731.2:c.2323C>T	XP_011537033.1:p.Gln775Ter
XM_017019961.1:c.2188C>T	XP_016875450.1:p.Gln730Ter
XM_017019962.2:c.1177C>T	XP_016875451.1:p.Gln393Ter