Canonical Allele Identifier: CA481577242

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102164190T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770412T>A , CM000674.2:g.101770412T>A	GRCh38
NC_000012.11:g.102164190T>A , CM000674.1:g.102164190T>A	GRCh37
NC_000012.10:g.100688321T>A	NCBI36
NG_021243.1:g.65456A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.1107A>T MANE Select	ENSP00000299314.7:p.Thr369=
ENST00000299314.11:c.1107A>T	ENSP00000299314.7:p.Thr369=
ENST00000549940.5:c.1107A>T	ENSP00000449150.1:p.Thr369=
NM_024312.4:c.1107A>T	NP_077288.2:p.Thr369=
XM_006719593.2:c.1107A>T	XP_006719656.1:p.Thr369=
XM_011538731.1:c.1026A>T	XP_011537033.1:p.Thr342=
XM_006719593.3:c.1107A>T	XP_006719656.1:p.Thr369=
XM_011538731.2:c.1026A>T	XP_011537033.1:p.Thr342=
XM_017019961.1:c.891A>T	XP_016875450.1:p.Thr297=
XM_017019962.2:c.-121A>T	XP_016875451.1:n.-121A>T
NM_024312.5:c.1107A>T MANE Select	NP_077288.2:p.Thr369=