Canonical Allele Identifier: CA481326239

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101786073-A-G
• MyVariant Identifiers: chr12:g.102179851A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786073A>G , CM000674.2:g.101786073A>G	GRCh38
NC_000012.11:g.102179851A>G , CM000674.1:g.102179851A>G	GRCh37
NC_000012.10:g.100703982A>G	NCBI36
NG_021243.1:g.49795T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.510T>C MANE Select	ENSP00000299314.7:p.Val170=
ENST00000299314.11:c.510T>C	ENSP00000299314.7:p.Val170=
ENST00000549940.5:c.510T>C	ENSP00000449150.1:p.Val170=
ENST00000550352.1:n.304T>C
ENST00000552681.1:c.144T>C	ENSP00000449217.1:p.Val48=
NM_024312.4:c.510T>C	NP_077288.2:p.Val170=
XM_006719593.2:c.510T>C	XP_006719656.1:p.Val170=
XM_011538731.1:c.429T>C	XP_011537033.1:p.Val143=
XM_006719593.3:c.510T>C	XP_006719656.1:p.Val170=
XM_011538731.2:c.429T>C	XP_011537033.1:p.Val143=
XM_017019961.1:c.294T>C	XP_016875450.1:p.Val98=
XM_017019962.2:c.-841T>C	XP_016875451.1:n.-841T>C
NM_024312.5:c.510T>C MANE Select	NP_077288.2:p.Val170=