Canonical Allele Identifier: CA2613847728

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446323-C-CCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446324_61446325insCTGTC , CM000673.2:g.61446324_61446325insCTGTC	GRCh38
NC_000011.9:g.61213796_61213797insCTGTC , CM000673.1:g.61213796_61213797insCTGTC	GRCh37
NC_000011.8:g.60970372_60970373insCTGTC	NCBI36
NG_023393.1:g.21200_21201insCTGTC , LRG_519:g.21200_21201insCTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*253_*254insCTGTC MANE Select	ENSP00000301761.3:n.*253_*254insCTGTC
ENST00000301761.6:c.*253_*254insCTGTC	ENSP00000301761.2:n.*253_*254insCTGTC
ENST00000536670.5:n.396+8211_396+8212insCTGTC
ENST00000538594.5:c.370+8211_370+8212insCTGTC	ENSP00000440939.1:n.370+8211_370+8212insCTGTC
ENST00000541135.5:c.377+8204_377+8205insCTGTC	ENSP00000443130.1:n.377+8204_377+8205insCTGTC
ENST00000542074.1:c.*333_*334insCTGTC	ENSP00000469670.1:n.*333_*334insCTGTC
ENST00000542794.5:c.*756_*757insCTGTC	ENSP00000439983.1:n.*756_*757insCTGTC
ENST00000543044.2:c.*160+93_*160+94insCTGTC	ENSP00000440219.1:n.*160+93_*160+94insCTGTC
ENST00000544025.5:n.465+8211_465+8212insCTGTC
ENST00000544801.5:c.370+8211_370+8212insCTGTC	ENSP00000442581.1:n.370+8211_370+8212insCTGTC
ENST00000544880.1:n.374+8211_374+8212insCTGTC
NM_017841.2:c.*253_*254insCTGTC , LRG_519t1:c.*253_*254insCTGTC	NP_060311.1:n.*253_*254insCTGTC
NM_017841.4:c.*253_*254insCTGTC MANE Select	NP_060311.1:n.*253_*254insCTGTC