Canonical Allele Identifier: CA920111401
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs1599953468

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411113_41411114insA , CM000681.2:g.41411113_41411114insA GRCh38
NC_000019.9:g.41917018_41917019insA , CM000681.1:g.41917018_41917019insA GRCh37
NC_000019.8:g.46608858_46608859insA NCBI36
NG_013004.1:g.18325_18326insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+104_375+105insA MANE Select ENSP00000269980.2:n.375+104_375+105insA
ENST00000269980.6:c.375+104_375+105insA ENSP00000269980.2:n.375+104_375+105insA
ENST00000457836.6:c.309+104_309+105insA ENSP00000416000.2:n.309+104_309+105insA
ENST00000538423.5:n.501+104_501+105insA
ENST00000540732.3:c.477+104_477+105insA ENSP00000443246.1:n.477+104_477+105insA
ENST00000541315.1:c.182+104_182+105insA
ENST00000542943.5:c.288+297_288+298insA ENSP00000440345.1:n.288+297_288+298insA
ENST00000595085.5:c.375+104_375+105insA ENSP00000471150.2:n.375+104_375+105insA
NM_000709.3:c.375+104_375+105insA NP_000700.1:n.375+104_375+105insA
NM_001164783.1:c.375+104_375+105insA NP_001158255.1:n.375+104_375+105insA
NM_000709.4:c.375+104_375+105insA MANE Select NP_000700.1:n.375+104_375+105insA
NM_001164783.2:c.375+104_375+105insA NP_001158255.1:n.375+104_375+105insA