Canonical Allele Identifier: CA2613847759
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446363_61446366dup , CM000673.2:g.61446363_61446366dup GRCh38
NC_000011.9:g.61213835_61213838dup , CM000673.1:g.61213835_61213838dup GRCh37
NC_000011.8:g.60970411_60970414dup NCBI36
NG_023393.1:g.21239_21242dup , LRG_519:g.21239_21242dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*292_*295dup MANE Select ENSP00000301761.3:n.*292_*295dup
ENST00000301761.6:c.*292_*295dup ENSP00000301761.2:n.*292_*295dup
ENST00000536670.5:n.396+8250_396+8253dup
ENST00000538594.5:c.370+8250_370+8253dup ENSP00000440939.1:n.370+8250_370+8253dup
ENST00000541135.5:c.377+8243_377+8246dup ENSP00000443130.1:n.377+8243_377+8246dup
ENST00000542074.1:c.*372_*375dup ENSP00000469670.1:n.*372_*375dup
ENST00000543044.2:c.*160+132_*160+135dup ENSP00000440219.1:n.*160+132_*160+135dup
ENST00000544025.5:n.465+8250_465+8253dup
ENST00000544801.5:c.370+8250_370+8253dup ENSP00000442581.1:n.370+8250_370+8253dup
ENST00000544880.1:n.374+8250_374+8253dup
NM_017841.2:c.*292_*295dup , LRG_519t1:c.*292_*295dup NP_060311.1:n.*292_*295dup
NM_017841.4:c.*292_*295dup MANE Select NP_060311.1:n.*292_*295dup