Canonical Allele Identifier: CA386294658

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153845A>T (hg19) ; chr12:g.101760067A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760067A>T , CM000674.2:g.101760067A>T	GRCh38
NC_000012.11:g.102153845A>T , CM000674.1:g.102153845A>T	GRCh37
NC_000012.10:g.100677976A>T	NCBI36
NG_021243.1:g.75801T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3212T>A MANE Select	ENSP00000299314.7:p.Ile1071Asn
ENST00000299314.11:c.3212T>A	ENSP00000299314.7:p.Ile1071Asn
ENST00000549194.1:n.78T>A
ENST00000550718.1:c.24T>A
NM_024312.4:c.3212T>A	NP_077288.2:p.Ile1071Asn
XM_006719593.2:c.3212T>A	XP_006719656.1:p.Ile1071Asn
XM_011538731.1:c.3131T>A	XP_011537033.1:p.Ile1044Asn
XM_006719593.3:c.3212T>A	XP_006719656.1:p.Ile1071Asn
XM_011538731.2:c.3131T>A	XP_011537033.1:p.Ile1044Asn
XM_017019961.1:c.2996T>A	XP_016875450.1:p.Ile999Asn
XM_017019962.2:c.1985T>A	XP_016875451.1:p.Ile662Asn
NM_024312.5:c.3212T>A MANE Select	NP_077288.2:p.Ile1071Asn