Canonical Allele Identifier: CA339964784

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43408925T>G (hg19) ; chr1:g.42943254T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42943254T>G , CM000663.2:g.42943254T>G	GRCh38
NC_000001.10:g.43408925T>G , CM000663.1:g.43408925T>G	GRCh37
NC_000001.9:g.43181512T>G	NCBI36
NG_008232.1:g.20923A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.86A>C MANE Select	ENSP00000416293.2:p.Asn29Thr
ENST00000674765.1:c.86A>C	ENSP00000501811.1:p.Asn29Thr
ENST00000675112.1:n.109A>C
ENST00000372500.4:c.19-12048A>C	ENSP00000361578.4:n.19-12048A>C
ENST00000415851.6:n.303A>C
ENST00000426263.7:c.86A>C	ENSP00000416293.2:p.Asn29Thr
ENST00000625233.2:n.294A>C
ENST00000628173.1:n.305A>C
ENST00000630287.2:c.86A>C	ENSP00000486694.1:p.Asn29Thr
ENST00000630821.1:n.303A>C
NM_006516.2:c.86A>C	NP_006507.2:p.Asn29Thr
NM_006516.3:c.86A>C	NP_006507.2:p.Asn29Thr
NM_006516.4:c.86A>C MANE Select	NP_006507.2:p.Asn29Thr