Canonical Allele Identifier: CA386297508

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102158024A>C (hg19) ; chr12:g.101764246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101764246A>C , CM000674.2:g.101764246A>C	GRCh38
NC_000012.11:g.102158024A>C , CM000674.1:g.102158024A>C	GRCh37
NC_000012.10:g.100682155A>C	NCBI36
NG_021243.1:g.71622T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.2671T>G MANE Select	ENSP00000299314.7:p.Phe891Val
ENST00000299314.11:c.2671T>G	ENSP00000299314.7:p.Phe891Val
NM_024312.4:c.2671T>G	NP_077288.2:p.Phe891Val
XM_006719593.2:c.2671T>G	XP_006719656.1:p.Phe891Val
XM_011538731.1:c.2590T>G	XP_011537033.1:p.Phe864Val
XM_006719593.3:c.2671T>G	XP_006719656.1:p.Phe891Val
XM_011538731.2:c.2590T>G	XP_011537033.1:p.Phe864Val
XM_017019961.1:c.2455T>G	XP_016875450.1:p.Phe819Val
XM_017019962.2:c.1444T>G	XP_016875451.1:p.Phe482Val
NM_024312.5:c.2671T>G MANE Select	NP_077288.2:p.Phe891Val