Canonical Allele Identifier: CA382617184
Gene: SDHD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088884T>C , CM000673.2:g.112088884T>C GRCh38
NC_000011.9:g.111959608T>C , CM000673.1:g.111959608T>C GRCh37
NC_000011.8:g.111464818T>C NCBI36
NG_012337.2:g.7038T>C
NG_033145.1:g.2915A>G
NG_012337.3:g.7038T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.187T>C ENSP00000432946.2:p.Ser63Pro
ENST00000534010.2:c.187T>C ENSP00000433202.2:p.Ser63Pro
ENST00000375549.8:c.187T>C MANE Select ENSP00000364699.3:p.Ser63Pro
ENST00000528021.6:c.187T>C ENSP00000432465.1:p.Ser63Pro
ENST00000640554.1:c.*259T>C ENSP00000491141.1:n.*259T>C
ENST00000375549.7:c.187T>C ENSP00000364699.3:p.Ser63Pro
ENST00000525291.5:c.70T>C ENSP00000436669.1:p.Ser24Pro
ENST00000525987.5:n.192T>C
ENST00000526592.5:c.187T>C ENSP00000432005.1:p.Ser63Pro
ENST00000528021.5:c.187T>C ENSP00000432465.1:p.Ser63Pro
ENST00000528048.5:c.169+911T>C ENSP00000436217.1:n.169+911T>C
ENST00000528182.5:c.187T>C ENSP00000435475.1:p.Ser63Pro
ENST00000530923.5:c.177T>C
ENST00000531744.5:c.187T>C ENSP00000456957.1:p.Ser63Pro
ENST00000532699.1:c.187T>C ENSP00000456434.1:p.Ser63Pro
ENST00000534010.1:c.18T>C
ENST00000614349.4:c.187T>C ENSP00000480666.1:p.Ser63Pro
NM_001276503.1:c.169+911T>C NP_001263432.1:n.169+911T>C
NM_001276504.1:c.70T>C NP_001263433.1:p.Ser24Pro
NM_001276506.1:c.187T>C NP_001263435.1:p.Ser63Pro
NM_003002.3:c.187T>C NP_002993.1:p.Ser63Pro
NR_077060.1:n.271T>C
NM_003002.4:c.187T>C MANE Select NP_002993.1:p.Ser63Pro
NM_001276503.2:c.169+911T>C NP_001263432.1:n.169+911T>C
NM_001276504.2:c.70T>C NP_001263433.1:p.Ser24Pro
NM_001276506.2:c.187T>C NP_001263435.1:p.Ser63Pro
NR_077060.2:n.222T>C