Canonical Allele Identifier: CA386305715

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102190488C>T (hg19) ; chr12:g.101796710C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796710C>T , CM000674.2:g.101796710C>T	GRCh38
NC_000012.11:g.102190488C>T , CM000674.1:g.102190488C>T	GRCh37
NC_000012.10:g.100714619C>T	NCBI36
NG_021243.1:g.39158G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.170G>A MANE Select	ENSP00000299314.7:p.Arg57Lys
ENST00000647144.1:n.290G>A
ENST00000299314.11:c.170G>A	ENSP00000299314.7:p.Arg57Lys
ENST00000392919.4:c.170G>A	ENSP00000376651.4:p.Arg57Lys
ENST00000549165.1:c.170G>A	ENSP00000450413.1:p.Arg57Lys
ENST00000549940.5:c.170G>A	ENSP00000449150.1:p.Arg57Lys
NM_024312.4:c.170G>A	NP_077288.2:p.Arg57Lys
XM_006719593.2:c.170G>A	XP_006719656.1:p.Arg57Lys
XM_011538731.1:c.89G>A	XP_011537033.1:p.Arg30Lys
XM_006719593.3:c.170G>A	XP_006719656.1:p.Arg57Lys
XM_011538731.2:c.89G>A	XP_011537033.1:p.Arg30Lys
XM_017019961.1:c.-47G>A	XP_016875450.1:n.-47G>A
XM_017019962.2:c.-1181G>A	XP_016875451.1:n.-1181G>A
NM_024312.5:c.170G>A MANE Select	NP_077288.2:p.Arg57Lys