Canonical Allele Identifier: CA386304827

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179816A>G (hg19) ; chr12:g.101786038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786038A>G , CM000674.2:g.101786038A>G	GRCh38
NC_000012.11:g.102179816A>G , CM000674.1:g.102179816A>G	GRCh37
NC_000012.10:g.100703947A>G	NCBI36
NG_021243.1:g.49830T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.545T>C MANE Select	ENSP00000299314.7:p.Val182Ala
ENST00000299314.11:c.545T>C	ENSP00000299314.7:p.Val182Ala
ENST00000549940.5:c.545T>C	ENSP00000449150.1:p.Val182Ala
ENST00000550352.1:n.339T>C
ENST00000552681.1:c.179T>C	ENSP00000449217.1:p.Val60Ala
NM_024312.4:c.545T>C	NP_077288.2:p.Val182Ala
XM_006719593.2:c.545T>C	XP_006719656.1:p.Val182Ala
XM_011538731.1:c.464T>C	XP_011537033.1:p.Val155Ala
XM_006719593.3:c.545T>C	XP_006719656.1:p.Val182Ala
XM_011538731.2:c.464T>C	XP_011537033.1:p.Val155Ala
XM_017019961.1:c.329T>C	XP_016875450.1:p.Val110Ala
XM_017019962.2:c.-806T>C	XP_016875451.1:n.-806T>C
NM_024312.5:c.545T>C MANE Select	NP_077288.2:p.Val182Ala