Canonical Allele Identifier: CA1165412757
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930681_42930750delinsCCACGAAGGGCTGTGGGTGACACTTCACCCACATACATGGGCACGAAGCCTGTGGTCAGGCCGCAGTACA , CM000663.2:g.42930681_42930750delinsCCACGAAGGGCTGTGGGTGACACTTCACCCACATACATGGGCACGAAGCCTGTGGTCAGGCCGCAGTACA GRCh38
NC_000001.10:g.43396352_43396421delinsCCACGAAGGGCTGTGGGTGACACTTCACCCACATACATGGGCACGAAGCCTGTGGTCAGGCCGCAGTACA , CM000663.1:g.43396352_43396421delinsCCACGAAGGGCTGTGGGTGACACTTCACCCACATACATGGGCACGAAGCCTGTGGTCAGGCCGCAGTACA GRCh37
NC_000001.9:g.43168939_43169008delinsCCACGAAGGGCTGTGGGTGACACTTCACCCACATACATGGGCACGAAGCCTGTGGTCAGGCCGCAGTACA NCBI36
NG_008232.1:g.33427_33496delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG MANE Select ENSP00000416293.2:p.Val131=
ENST00000674765.1:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG ENSP00000501811.1:p.Val131=
ENST00000675112.1:n.415_484delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG
ENST00000676254.1:n.841_910delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG
ENST00000426263.7:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG ENSP00000416293.2:p.Val131=
ENST00000439722.2:c.271_340delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG ENSP00000395521.2:n.271_340delinsTGTACTGCGGCCTGACCACAGGCTTCGT...
ENST00000475162.3:c.291_360delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG
ENST00000625233.2:n.600_669delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG
ENST00000630287.2:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG ENSP00000486694.1:p.Val131=
NM_006516.2:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG NP_006507.2:p.Val131=
NM_006516.3:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG NP_006507.2:p.Val131=
NM_006516.4:c.392_461delinsTGTACTGCGGCCTGACCACAGGCTTCGTGCCCATGTATGTGGGTGAAGTGTCACCCACAGCCCTTCGTGG MANE Select NP_006507.2:p.Val131=