Canonical Allele Identifier: CA386303151

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102164258A>T (hg19) ; chr12:g.101770480A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770480A>T , CM000674.2:g.101770480A>T	GRCh38
NC_000012.11:g.102164258A>T , CM000674.1:g.102164258A>T	GRCh37
NC_000012.10:g.100688389A>T	NCBI36
NG_021243.1:g.65388T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1039T>A MANE Select	ENSP00000299314.7:p.Phe347Ile
ENST00000299314.11:c.1039T>A	ENSP00000299314.7:p.Phe347Ile
ENST00000549940.5:c.1039T>A	ENSP00000449150.1:p.Phe347Ile
NM_024312.4:c.1039T>A	NP_077288.2:p.Phe347Ile
XM_006719593.2:c.1039T>A	XP_006719656.1:p.Phe347Ile
XM_011538731.1:c.958T>A	XP_011537033.1:p.Phe320Ile
XM_006719593.3:c.1039T>A	XP_006719656.1:p.Phe347Ile
XM_011538731.2:c.958T>A	XP_011537033.1:p.Phe320Ile
XM_017019961.1:c.823T>A	XP_016875450.1:p.Phe275Ile
XM_017019962.2:c.-189T>A	XP_016875451.1:n.-189T>A
NM_024312.5:c.1039T>A MANE Select	NP_077288.2:p.Phe347Ile