Canonical Allele Identifier: CA339955439

Gene: SLC2A1

Linked Data

• dbSNP Id: rs1325117168
• MyVariant Identifiers: chr1:g.43394601A>T (hg19) ; chr1:g.42928930A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42928930A>T , CM000663.2:g.42928930A>T	GRCh38
NC_000001.10:g.43394601A>T , CM000663.1:g.43394601A>T	GRCh37
NC_000001.9:g.43167188A>T	NCBI36
NG_008232.1:g.35247T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1074+2T>A MANE Select	ENSP00000416293.2:n.1074+2T>A
ENST00000674545.1:n.570T>A
ENST00000674765.1:c.1029+47T>A	ENSP00000501811.1:n.1029+47T>A
ENST00000675112.1:n.1375+2T>A
ENST00000676254.1:n.1523+2T>A
ENST00000426263.7:c.1074+2T>A	ENSP00000416293.2:n.1074+2T>A
ENST00000475162.3:c.415+1696T>A
ENST00000630287.2:c.*389+2T>A	ENSP00000486694.1:n.*389+2T>A
NM_006516.2:c.1074+2T>A	NP_006507.2:n.1074+2T>A
NM_006516.3:c.1074+2T>A	NP_006507.2:n.1074+2T>A
NM_006516.4:c.1074+2T>A MANE Select	NP_006507.2:n.1074+2T>A