Canonical Allele Identifier: CA2668526362

Gene: SLC2A2

Linked Data

• gnomAD v4: 3-171014428-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171014428A>G , CM000665.2:g.171014428A>G	GRCh38
NC_000003.11:g.170732217A>G , CM000665.1:g.170732217A>G	GRCh37
NC_000003.10:g.172214911A>G	NCBI36
NG_008108.1:g.17552T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.371+41T>C MANE Select	ENSP00000323568.3:n.371+41T>C
ENST00000314251.7:c.371+41T>C	ENSP00000323568.3:n.371+41T>C
ENST00000461867.1:c.-24+4103T>C	ENSP00000418888.1:n.-24+4103T>C
ENST00000469787.1:c.108+4103T>C	ENSP00000417918.1:n.108+4103T>C
ENST00000497642.5:c.371+41T>C	ENSP00000418456.1:n.371+41T>C
NM_000340.1:c.371+41T>C	NP_000331.1:n.371+41T>C
NM_001278658.1:c.14+4103T>C	NP_001265587.1:n.14+4103T>C
NM_001278659.1:c.-24+41T>C	NP_001265588.1:n.-24+41T>C
XM_011513087.1:c.326+41T>C	XP_011511389.1:n.326+41T>C
XM_011513088.1:c.152+41T>C	XP_011511390.1:n.152+41T>C
XM_011513089.1:c.-24+4103T>C	XP_011511391.1:n.-24+4103T>C
XM_011513087.2:c.326+41T>C	XP_011511389.1:n.326+41T>C
XM_024453720.1:c.-24+4103T>C	XP_024309488.1:n.-24+4103T>C
NM_000340.2:c.371+41T>C MANE Select	NP_000331.1:n.371+41T>C
NM_001278658.2:c.14+4103T>C	NP_001265587.1:n.14+4103T>C
NM_001278659.2:c.-24+41T>C	NP_001265588.1:n.-24+41T>C