Canonical Allele Identifier: CA339961029

Gene: SLC2A1

Linked Data

• gnomAD v4: 1-42930779-C-A
• MyVariant Identifiers: chr1:g.43396450C>A (hg19) ; chr1:g.42930779C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42930779C>A , CM000663.2:g.42930779C>A	GRCh38
NC_000001.10:g.43396450C>A , CM000663.1:g.43396450C>A	GRCh37
NC_000001.9:g.43169037C>A	NCBI36
NG_008232.1:g.33398G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.363G>T MANE Select	ENSP00000416293.2:p.Met121Ile
ENST00000674765.1:c.363G>T	ENSP00000501811.1:p.Met121Ile
ENST00000675112.1:n.386G>T
ENST00000676254.1:n.812G>T
ENST00000372500.4:c.267G>T	ENSP00000361578.4:p.Met89Ile
ENST00000426263.7:c.363G>T	ENSP00000416293.2:p.Met121Ile
ENST00000439722.2:c.242G>T	ENSP00000395521.2:n.242G>T
ENST00000475162.3:c.262G>T
ENST00000625233.2:n.571G>T
ENST00000630287.2:c.363G>T	ENSP00000486694.1:p.Met121Ile
NM_006516.2:c.363G>T	NP_006507.2:p.Met121Ile
NM_006516.3:c.363G>T	NP_006507.2:p.Met121Ile
NM_006516.4:c.363G>T MANE Select	NP_006507.2:p.Met121Ile