Canonical Allele Identifier: CA8021717
Gene: BCKDK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31111297T>C , CM000678.2:g.31111297T>C GRCh38
NC_000016.9:g.31122618T>C , CM000678.1:g.31122618T>C GRCh37
NC_000016.8:g.31030119T>C NCBI36
NG_033011.1:g.8004T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005881.4:c.846-3T>C MANE Select NP_005872.2:n.846-3T>C
ENST00000219794.11:c.846-3T>C MANE Select ENSP00000219794.6:n.846-3T>C
NM_001122957.2:c.846-3T>C NP_001116429.1:n.846-3T>C
NM_001122957.3:c.846-3T>C NP_001116429.1:n.846-3T>C
NM_001122957.4:c.846-3T>C NP_001116429.1:n.846-3T>C
NM_001271926.1:c.845+78T>C NP_001258855.1:n.845+78T>C
NM_001271926.2:c.845+78T>C NP_001258855.1:n.845+78T>C
NM_001271926.3:c.845+78T>C NP_001258855.1:n.845+78T>C
NM_005881.3:c.846-3T>C NP_005872.2:n.846-3T>C
ENST00000219794.10:c.846-3T>C ENSP00000219794.6:n.846-3T>C
ENST00000287507.7:c.845+78T>C ENSP00000287507.3:n.845+78T>C
ENST00000394950.7:c.846-3T>C ENSP00000378404.3:n.846-3T>C
ENST00000394951.5:c.846-3T>C ENSP00000378405.1:n.846-3T>C
ENST00000566568.1:n.1864-3T>C
ENST00000567530.5:c.*118-3T>C ENSP00000456479.1:n.*118-3T>C
XM_017022859.1:c.846-3T>C XP_016878348.1:n.846-3T>C