Canonical Allele Identifier: CA645509537

Gene: SDHD

Linked Data

• ClinVar Variation Id: 438441
• ClinVar RCV Id: RCV000505280

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086908_112087973del , CM000673.2:g.112086908_112087973del	GRCh38
NC_000011.9:g.111957632_111958697del , CM000673.1:g.111957632_111958697del	GRCh37
NC_000011.8:g.111462842_111463907del	NCBI36
NG_012337.2:g.5062_6127del
NG_033145.1:g.3826_4891del
NG_012337.3:g.5062_6127del

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.1_169del
ENST00000534010.2:c.1_169del
ENST00000375549.8:c.1_169del
ENST00000528021.6:c.1_169del
ENST00000640554.1:c.1_169del
ENST00000375549.7:c.1_169del
ENST00000525291.5:c.1_53-894del
ENST00000525987.5:n.6_174del
ENST00000526592.5:c.1_169del
ENST00000528021.5:c.1_169del
ENST00000528048.5:c.1_169del
ENST00000528182.5:c.1_169del
ENST00000531744.5:c.1_169del
ENST00000532699.1:c.1_169del
ENST00000614349.4:c.1_169del
NM_001276503.1:c.1_169del
NM_001276504.1:c.1_53-894del
NM_001276506.1:c.1_169del
NM_003002.3:c.1_169del
NR_077060.1:n.85_253del
NM_003002.4:c.1_169del
NM_001276503.2:c.1_169del
NM_001276504.2:c.1_53-894del
NM_001276506.2:c.1_169del
NR_077060.2:n.36_204del