Canonical Allele Identifier: CA386305826

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102190537C>T (hg19) ; chr12:g.101796759C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796759C>T , CM000674.2:g.101796759C>T	GRCh38
NC_000012.11:g.102190537C>T , CM000674.1:g.102190537C>T	GRCh37
NC_000012.10:g.100714668C>T	NCBI36
NG_021243.1:g.39109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.121G>A MANE Select	ENSP00000299314.7:p.Val41Ile
ENST00000647144.1:n.241G>A
ENST00000299314.11:c.121G>A	ENSP00000299314.7:p.Val41Ile
ENST00000392919.4:c.121G>A	ENSP00000376651.4:p.Val41Ile
ENST00000549165.1:c.121G>A	ENSP00000450413.1:p.Val41Ile
ENST00000549940.5:c.121G>A	ENSP00000449150.1:p.Val41Ile
NM_024312.4:c.121G>A	NP_077288.2:p.Val41Ile
XM_006719593.2:c.121G>A	XP_006719656.1:p.Val41Ile
XM_011538731.1:c.40G>A	XP_011537033.1:p.Val14Ile
XM_006719593.3:c.121G>A	XP_006719656.1:p.Val41Ile
XM_011538731.2:c.40G>A	XP_011537033.1:p.Val14Ile
XM_017019961.1:c.-96G>A	XP_016875450.1:n.-96G>A
XM_017019962.2:c.-1230G>A	XP_016875451.1:n.-1230G>A
NM_024312.5:c.121G>A MANE Select	NP_077288.2:p.Val41Ile