Canonical Allele Identifier: CA386305752

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102190506A>C (hg19) ; chr12:g.101796728A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796728A>C , CM000674.2:g.101796728A>C	GRCh38
NC_000012.11:g.102190506A>C , CM000674.1:g.102190506A>C	GRCh37
NC_000012.10:g.100714637A>C	NCBI36
NG_021243.1:g.39140T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.152T>G MANE Select	ENSP00000299314.7:p.Val51Gly
ENST00000647144.1:n.272T>G
ENST00000299314.11:c.152T>G	ENSP00000299314.7:p.Val51Gly
ENST00000392919.4:c.152T>G	ENSP00000376651.4:p.Val51Gly
ENST00000549165.1:c.152T>G	ENSP00000450413.1:p.Val51Gly
ENST00000549940.5:c.152T>G	ENSP00000449150.1:p.Val51Gly
NM_024312.4:c.152T>G	NP_077288.2:p.Val51Gly
XM_006719593.2:c.152T>G	XP_006719656.1:p.Val51Gly
XM_011538731.1:c.71T>G	XP_011537033.1:p.Val24Gly
XM_006719593.3:c.152T>G	XP_006719656.1:p.Val51Gly
XM_011538731.2:c.71T>G	XP_011537033.1:p.Val24Gly
XM_017019961.1:c.-65T>G	XP_016875450.1:n.-65T>G
XM_017019962.2:c.-1199T>G	XP_016875451.1:n.-1199T>G
NM_024312.5:c.152T>G MANE Select	NP_077288.2:p.Val51Gly