Canonical Allele Identifier: CA386294720

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153860G>T (hg19) ; chr12:g.101760082G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760082G>T , CM000674.2:g.101760082G>T	GRCh38
NC_000012.11:g.102153860G>T , CM000674.1:g.102153860G>T	GRCh37
NC_000012.10:g.100677991G>T	NCBI36
NG_021243.1:g.75786C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3197C>A MANE Select	ENSP00000299314.7:p.Thr1066Lys
ENST00000299314.11:c.3197C>A	ENSP00000299314.7:p.Thr1066Lys
ENST00000549194.1:n.63C>A
ENST00000550718.1:c.9C>A
NM_024312.4:c.3197C>A	NP_077288.2:p.Thr1066Lys
XM_006719593.2:c.3197C>A	XP_006719656.1:p.Thr1066Lys
XM_011538731.1:c.3116C>A	XP_011537033.1:p.Thr1039Lys
XM_006719593.3:c.3197C>A	XP_006719656.1:p.Thr1066Lys
XM_011538731.2:c.3116C>A	XP_011537033.1:p.Thr1039Lys
XM_017019961.1:c.2981C>A	XP_016875450.1:p.Thr994Lys
XM_017019962.2:c.1970C>A	XP_016875451.1:p.Thr657Lys
NM_024312.5:c.3197C>A MANE Select	NP_077288.2:p.Thr1066Lys