Canonical Allele Identifier: CA386294642

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153837T>A (hg19) ; chr12:g.101760059T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760059T>A , CM000674.2:g.101760059T>A	GRCh38
NC_000012.11:g.102153837T>A , CM000674.1:g.102153837T>A	GRCh37
NC_000012.10:g.100677968T>A	NCBI36
NG_021243.1:g.75809A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3220A>T MANE Select	ENSP00000299314.7:p.Thr1074Ser
ENST00000299314.11:c.3220A>T	ENSP00000299314.7:p.Thr1074Ser
ENST00000549194.1:n.86A>T
ENST00000550718.1:c.32A>T
NM_024312.4:c.3220A>T	NP_077288.2:p.Thr1074Ser
XM_006719593.2:c.3220A>T	XP_006719656.1:p.Thr1074Ser
XM_011538731.1:c.3139A>T	XP_011537033.1:p.Thr1047Ser
XM_006719593.3:c.3220A>T	XP_006719656.1:p.Thr1074Ser
XM_011538731.2:c.3139A>T	XP_011537033.1:p.Thr1047Ser
XM_017019961.1:c.3004A>T	XP_016875450.1:p.Thr1002Ser
XM_017019962.2:c.1993A>T	XP_016875451.1:p.Thr665Ser
NM_024312.5:c.3220A>T MANE Select	NP_077288.2:p.Thr1074Ser