Canonical Allele Identifier: CA916903664
Gene: PDHB HGNC NCBI

Linked Data

dbSNP Id: rs1553848494

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58431043_58431044insA , CM000665.2:g.58431043_58431044insA GRCh38
NC_000003.11:g.58416770_58416771insA , CM000665.1:g.58416770_58416771insA GRCh37
NC_000003.10:g.58391810_58391811insA NCBI36
NG_016860.1:g.7809_7810insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000302746.11:c.304-102_304-101insT MANE Select ENSP00000307241.6:n.304-102_304-101insT
ENST00000302746.10:c.304-102_304-101insT ENSP00000307241.6:n.304-102_304-101insT
ENST00000383714.8:c.250-102_250-101insT ENSP00000373220.4:n.250-102_250-101insT
ENST00000461692.5:n.417-102_417-101insT
ENST00000469364.5:c.304-102_304-101insT ENSP00000419580.1:n.304-102_304-101insT
ENST00000474765.1:c.250-102_250-101insT ENSP00000418448.1:n.250-102_250-101insT
ENST00000479945.1:n.2607_2608insT
ENST00000480626.5:n.396-102_396-101insT
ENST00000485460.5:c.304-102_304-101insT ENSP00000417267.1:n.304-102_304-101insT
NM_000925.3:c.304-102_304-101insT NP_000916.2:n.304-102_304-101insT
NM_001173468.1:c.304-102_304-101insT NP_001166939.1:n.304-102_304-101insT
NM_001315536.1:c.250-102_250-101insT NP_001302465.1:n.250-102_250-101insT
NR_033384.1:n.417-102_417-101insT
NM_000925.4:c.304-102_304-101insT MANE Select NP_000916.2:n.304-102_304-101insT
NM_001173468.2:c.304-102_304-101insT NP_001166939.1:n.304-102_304-101insT
NM_001315536.2:c.250-102_250-101insT NP_001302465.1:n.250-102_250-101insT
NR_033384.2:n.410-102_410-101insT