Canonical Allele Identifier: CA481326191

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179815A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786037A>T , CM000674.2:g.101786037A>T	GRCh38
NC_000012.11:g.102179815A>T , CM000674.1:g.102179815A>T	GRCh37
NC_000012.10:g.100703946A>T	NCBI36
NG_021243.1:g.49831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.546T>A MANE Select	ENSP00000299314.7:p.Val182=
ENST00000299314.11:c.546T>A	ENSP00000299314.7:p.Val182=
ENST00000549940.5:c.546T>A	ENSP00000449150.1:p.Val182=
ENST00000550352.1:n.340T>A
ENST00000552681.1:c.180T>A	ENSP00000449217.1:p.Val60=
NM_024312.4:c.546T>A	NP_077288.2:p.Val182=
XM_006719593.2:c.546T>A	XP_006719656.1:p.Val182=
XM_011538731.1:c.465T>A	XP_011537033.1:p.Val155=
XM_006719593.3:c.546T>A	XP_006719656.1:p.Val182=
XM_011538731.2:c.465T>A	XP_011537033.1:p.Val155=
XM_017019961.1:c.330T>A	XP_016875450.1:p.Val110=
XM_017019962.2:c.-805T>A	XP_016875451.1:n.-805T>A
NM_024312.5:c.546T>A MANE Select	NP_077288.2:p.Val182=