Canonical Allele Identifier: CA2695215319
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088899dup , CM000673.2:g.112088899dup GRCh38
NC_000011.9:g.111959623dup , CM000673.1:g.111959623dup GRCh37
NC_000011.8:g.111464833dup NCBI36
NG_012337.2:g.7053dup
NG_033145.1:g.2900dup
NG_012337.3:g.7053dup

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.202dup ENSP00000432946.2:p.Ser68LysfsTer?
ENST00000534010.2:c.202dup ENSP00000433202.2:p.Ser68LysfsTer?
ENST00000375549.8:c.202dup MANE Select ENSP00000364699.3:p.Ser68LysfsTer?
ENST00000528021.6:c.202dup ENSP00000432465.1:p.Ser68LysfsTer?
ENST00000640554.1:c.*274dup ENSP00000491141.1:n.*274dup
ENST00000375549.7:c.202dup ENSP00000364699.3:p.Ser68LysfsTer?
ENST00000525291.5:c.85dup ENSP00000436669.1:p.Ser29LysfsTer?
ENST00000525987.5:n.207dup
ENST00000526592.5:c.202dup ENSP00000432005.1:p.Ser68LysfsTer?
ENST00000528021.5:c.202dup ENSP00000432465.1:p.Ser68LysfsTer?
ENST00000528048.5:c.169+926dup ENSP00000436217.1:n.169+926dup
ENST00000528182.5:c.202dup ENSP00000435475.1:p.Ser68LysfsTer?
ENST00000530923.5:c.192dup
ENST00000531744.5:c.202dup ENSP00000456957.1:p.Ser68LysfsTer?
ENST00000532699.1:c.202dup ENSP00000456434.1:p.Ser68LysfsTer?
ENST00000534010.1:c.33dup
ENST00000614349.4:c.202dup ENSP00000480666.1:p.Ser68LysfsTer?
NM_001276503.1:c.169+926dup NP_001263432.1:n.169+926dup
NM_001276504.1:c.85dup NP_001263433.1:p.Ser29LysfsTer?
NM_001276506.1:c.202dup NP_001263435.1:p.Ser68LysfsTer?
NM_003002.3:c.202dup NP_002993.1:p.Ser68LysfsTer?
NR_077060.1:n.286dup
NM_003002.4:c.202dup MANE Select NP_002993.1:p.Ser68LysfsTer?
NM_001276503.2:c.169+926dup NP_001263432.1:n.169+926dup
NM_001276504.2:c.85dup NP_001263433.1:p.Ser29LysfsTer?
NM_001276506.2:c.202dup NP_001263435.1:p.Ser68LysfsTer?
NR_077060.2:n.237dup