Canonical Allele Identifier: CA386304860

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179834G>T (hg19) ; chr12:g.101786056G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786056G>T , CM000674.2:g.101786056G>T	GRCh38
NC_000012.11:g.102179834G>T , CM000674.1:g.102179834G>T	GRCh37
NC_000012.10:g.100703965G>T	NCBI36
NG_021243.1:g.49812C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.527C>A MANE Select	ENSP00000299314.7:p.Pro176His
ENST00000299314.11:c.527C>A	ENSP00000299314.7:p.Pro176His
ENST00000549940.5:c.527C>A	ENSP00000449150.1:p.Pro176His
ENST00000550352.1:n.321C>A
ENST00000552681.1:c.161C>A	ENSP00000449217.1:p.Pro54His
NM_024312.4:c.527C>A	NP_077288.2:p.Pro176His
XM_006719593.2:c.527C>A	XP_006719656.1:p.Pro176His
XM_011538731.1:c.446C>A	XP_011537033.1:p.Pro149His
XM_006719593.3:c.527C>A	XP_006719656.1:p.Pro176His
XM_011538731.2:c.446C>A	XP_011537033.1:p.Pro149His
XM_017019961.1:c.311C>A	XP_016875450.1:p.Pro104His
XM_017019962.2:c.-824C>A	XP_016875451.1:n.-824C>A
NM_024312.5:c.527C>A MANE Select	NP_077288.2:p.Pro176His