Canonical Allele Identifier: CA1977301537
Gene: SDHAF2 HGNC NCBI

Linked Data

dbSNP Id: rs1862139799

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446454_61446456dup , CM000673.2:g.61446454_61446456dup GRCh38
NC_000011.9:g.61213926_61213928dup , CM000673.1:g.61213926_61213928dup GRCh37
NC_000011.8:g.60970502_60970504dup NCBI36
NG_023393.1:g.21330_21332dup , LRG_519:g.21330_21332dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*383_*385dup MANE Select ENSP00000301761.3:n.*383_*385dup
ENST00000301761.6:c.*383_*385dup ENSP00000301761.2:n.*383_*385dup
ENST00000536670.5:n.396+8341_396+8343dup
ENST00000538594.5:c.370+8341_370+8343dup ENSP00000440939.1:n.370+8341_370+8343dup
ENST00000541135.5:c.377+8334_377+8336dup ENSP00000443130.1:n.377+8334_377+8336dup
ENST00000542074.1:c.*463_*465dup ENSP00000469670.1:n.*463_*465dup
ENST00000543044.2:c.*160+223_*160+225dup ENSP00000440219.1:n.*160+223_*160+225dup
ENST00000544025.5:n.465+8341_465+8343dup
ENST00000544801.5:c.370+8341_370+8343dup ENSP00000442581.1:n.370+8341_370+8343dup
ENST00000544880.1:n.374+8341_374+8343dup
NM_017841.2:c.*383_*385dup , LRG_519t1:c.*383_*385dup NP_060311.1:n.*383_*385dup
NM_017841.4:c.*383_*385dup MANE Select NP_060311.1:n.*383_*385dup