Canonical Allele Identifier: CA481318555

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153892T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760114T>A , CM000674.2:g.101760114T>A	GRCh38
NC_000012.11:g.102153892T>A , CM000674.1:g.102153892T>A	GRCh37
NC_000012.10:g.100678023T>A	NCBI36
NG_021243.1:g.75754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3165A>T MANE Select	ENSP00000299314.7:p.Ile1055=
ENST00000299314.11:c.3165A>T	ENSP00000299314.7:p.Ile1055=
ENST00000549194.1:n.31A>T
NM_024312.4:c.3165A>T	NP_077288.2:p.Ile1055=
XM_006719593.2:c.3165A>T	XP_006719656.1:p.Ile1055=
XM_011538731.1:c.3084A>T	XP_011537033.1:p.Ile1028=
XM_006719593.3:c.3165A>T	XP_006719656.1:p.Ile1055=
XM_011538731.2:c.3084A>T	XP_011537033.1:p.Ile1028=
XM_017019961.1:c.2949A>T	XP_016875450.1:p.Ile983=
XM_017019962.2:c.1938A>T	XP_016875451.1:p.Ile646=
NM_024312.5:c.3165A>T MANE Select	NP_077288.2:p.Ile1055=