Canonical Allele Identifier: CA481577836

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102163832T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770054T>A , CM000674.2:g.101770054T>A	GRCh38
NC_000012.11:g.102163832T>A , CM000674.1:g.102163832T>A	GRCh37
NC_000012.10:g.100687963T>A	NCBI36
NG_021243.1:g.65814A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.1251A>T MANE Select	ENSP00000299314.7:p.Pro417=
ENST00000299314.11:c.1251A>T	ENSP00000299314.7:p.Pro417=
ENST00000549940.5:c.1251A>T	ENSP00000449150.1:p.Pro417=
NM_024312.4:c.1251A>T	NP_077288.2:p.Pro417=
XM_006719593.2:c.1251A>T	XP_006719656.1:p.Pro417=
XM_011538731.1:c.1170A>T	XP_011537033.1:p.Pro390=
XM_006719593.3:c.1251A>T	XP_006719656.1:p.Pro417=
XM_011538731.2:c.1170A>T	XP_011537033.1:p.Pro390=
XM_017019961.1:c.1035A>T	XP_016875450.1:p.Pro345=
XM_017019962.2:c.24A>T	XP_016875451.1:p.Pro8=
NM_024312.5:c.1251A>T MANE Select	NP_077288.2:p.Pro417=