Canonical Allele Identifier: CA2645198860
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42928929-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42928929C>T , CM000663.2:g.42928929C>T GRCh38
NC_000001.10:g.43394600C>T , CM000663.1:g.43394600C>T GRCh37
NC_000001.9:g.43167187C>T NCBI36
NG_008232.1:g.35248G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.1074+3G>A MANE Select ENSP00000416293.2:n.1074+3G>A
ENST00000674545.1:n.571G>A
ENST00000674765.1:c.1029+48G>A ENSP00000501811.1:n.1029+48G>A
ENST00000675112.1:n.1375+3G>A
ENST00000676254.1:n.1523+3G>A
ENST00000426263.7:c.1074+3G>A ENSP00000416293.2:n.1074+3G>A
ENST00000475162.3:c.415+1697G>A
ENST00000630287.2:c.*389+3G>A ENSP00000486694.1:n.*389+3G>A
NM_006516.2:c.1074+3G>A NP_006507.2:n.1074+3G>A
NM_006516.3:c.1074+3G>A NP_006507.2:n.1074+3G>A
NM_006516.4:c.1074+3G>A MANE Select NP_006507.2:n.1074+3G>A