Canonical Allele Identifier: CA1977301436
Gene: SDHAF2 HGNC NCBI

Linked Data

dbSNP Id: rs1862138147

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446355_61446356insTA , CM000673.2:g.61446355_61446356insTA GRCh38
NC_000011.9:g.61213827_61213828insTA , CM000673.1:g.61213827_61213828insTA GRCh37
NC_000011.8:g.60970403_60970404insTA NCBI36
NG_023393.1:g.21231_21232insTA , LRG_519:g.21231_21232insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*284_*285insTA MANE Select ENSP00000301761.3:n.*284_*285insTA
ENST00000301761.6:c.*284_*285insTA ENSP00000301761.2:n.*284_*285insTA
ENST00000536670.5:n.396+8242_396+8243insTA
ENST00000538594.5:c.370+8242_370+8243insTA ENSP00000440939.1:n.370+8242_370+8243insTA
ENST00000541135.5:c.377+8235_377+8236insTA ENSP00000443130.1:n.377+8235_377+8236insTA
ENST00000542074.1:c.*364_*365insTA ENSP00000469670.1:n.*364_*365insTA
ENST00000543044.2:c.*160+124_*160+125insTA ENSP00000440219.1:n.*160+124_*160+125insTA
ENST00000544025.5:n.465+8242_465+8243insTA
ENST00000544801.5:c.370+8242_370+8243insTA ENSP00000442581.1:n.370+8242_370+8243insTA
ENST00000544880.1:n.374+8242_374+8243insTA
NM_017841.2:c.*284_*285insTA , LRG_519t1:c.*284_*285insTA NP_060311.1:n.*284_*285insTA
NM_017841.4:c.*284_*285insTA MANE Select NP_060311.1:n.*284_*285insTA