Canonical Allele Identifier: CA2695215443
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086954_112086960del , CM000673.2:g.112086954_112086960del GRCh38
NC_000011.9:g.111957678_111957684del , CM000673.1:g.111957678_111957684del GRCh37
NC_000011.8:g.111462888_111462894del NCBI36
NG_012337.2:g.5108_5114del
NG_033145.1:g.4840_4846del
NG_012337.3:g.5108_5114del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.47_52+1del
ENST00000534010.2:c.47_52+1del
ENST00000375549.8:c.47_52+1del
ENST00000528021.6:c.47_52+1del
ENST00000640554.1:c.47_52+1del
ENST00000375549.7:c.47_52+1del
ENST00000525291.5:c.47_52+1del
ENST00000525987.5:n.52_57+1del
ENST00000526592.5:c.47_52+1del
ENST00000528021.5:c.47_52+1del
ENST00000528048.5:c.47_52+1del
ENST00000528182.5:c.47_52+1del
ENST00000530923.5:c.37_42+1del
ENST00000531744.5:c.47_52+1del
ENST00000532699.1:c.47_52+1del
ENST00000614349.4:c.47_52+1del
NM_001276503.1:c.47_52+1del
NM_001276504.1:c.47_52+1del
NM_001276506.1:c.47_52+1del
NM_003002.3:c.47_52+1del
NR_077060.1:n.131_136+1del
NM_003002.4:c.47_52+1del
NM_001276503.2:c.47_52+1del
NM_001276504.2:c.47_52+1del
NM_001276506.2:c.47_52+1del
NR_077060.2:n.82_87+1del