Canonical Allele Identifier: CA386294673

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153850A>T (hg19) ; chr12:g.101760072A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760072A>T , CM000674.2:g.101760072A>T	GRCh38
NC_000012.11:g.102153850A>T , CM000674.1:g.102153850A>T	GRCh37
NC_000012.10:g.100677981A>T	NCBI36
NG_021243.1:g.75796T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3207T>A MANE Select	ENSP00000299314.7:p.Asn1069Lys
ENST00000299314.11:c.3207T>A	ENSP00000299314.7:p.Asn1069Lys
ENST00000549194.1:n.73T>A
ENST00000550718.1:c.19T>A
NM_024312.4:c.3207T>A	NP_077288.2:p.Asn1069Lys
XM_006719593.2:c.3207T>A	XP_006719656.1:p.Asn1069Lys
XM_011538731.1:c.3126T>A	XP_011537033.1:p.Asn1042Lys
XM_006719593.3:c.3207T>A	XP_006719656.1:p.Asn1069Lys
XM_011538731.2:c.3126T>A	XP_011537033.1:p.Asn1042Lys
XM_017019961.1:c.2991T>A	XP_016875450.1:p.Asn997Lys
XM_017019962.2:c.1980T>A	XP_016875451.1:p.Asn660Lys
NM_024312.5:c.3207T>A MANE Select	NP_077288.2:p.Asn1069Lys