Canonical Allele Identifier: CA481576784

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155443T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761665T>G , CM000674.2:g.101761665T>G	GRCh38
NC_000012.11:g.102155443T>G , CM000674.1:g.102155443T>G	GRCh37
NC_000012.10:g.100679574T>G	NCBI36
NG_021243.1:g.74203A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2814A>C MANE Select	ENSP00000299314.7:p.Val938=
ENST00000299314.11:c.2814A>C	ENSP00000299314.7:p.Val938=
NM_024312.4:c.2814A>C	NP_077288.2:p.Val938=
XM_006719593.2:c.2814A>C	XP_006719656.1:p.Val938=
XM_011538731.1:c.2733A>C	XP_011537033.1:p.Val911=
XM_006719593.3:c.2814A>C	XP_006719656.1:p.Val938=
XM_011538731.2:c.2733A>C	XP_011537033.1:p.Val911=
XM_017019961.1:c.2598A>C	XP_016875450.1:p.Val866=
XM_017019962.2:c.1587A>C	XP_016875451.1:p.Val529=
NM_024312.5:c.2814A>C MANE Select	NP_077288.2:p.Val938=