Canonical Allele Identifier: CA481576813

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155464A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761686A>G , CM000674.2:g.101761686A>G	GRCh38
NC_000012.11:g.102155464A>G , CM000674.1:g.102155464A>G	GRCh37
NC_000012.10:g.100679595A>G	NCBI36
NG_021243.1:g.74182T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2793T>C MANE Select	ENSP00000299314.7:p.Phe931=
ENST00000299314.11:c.2793T>C	ENSP00000299314.7:p.Phe931=
NM_024312.4:c.2793T>C	NP_077288.2:p.Phe931=
XM_006719593.2:c.2793T>C	XP_006719656.1:p.Phe931=
XM_011538731.1:c.2712T>C	XP_011537033.1:p.Phe904=
XM_006719593.3:c.2793T>C	XP_006719656.1:p.Phe931=
XM_011538731.2:c.2712T>C	XP_011537033.1:p.Phe904=
XM_017019961.1:c.2577T>C	XP_016875450.1:p.Phe859=
XM_017019962.2:c.1566T>C	XP_016875451.1:p.Phe522=
NM_024312.5:c.2793T>C MANE Select	NP_077288.2:p.Phe931=