Canonical Allele Identifier: CA2679497873

Gene: BCKDHB

Linked Data

• gnomAD v4: 6-80168778-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168778A>C , CM000668.2:g.80168778A>C	GRCh38
NC_000006.11:g.80878495A>C , CM000668.1:g.80878495A>C	GRCh37
NC_000006.10:g.80935214A>C	NCBI36
NG_009775.1:g.67152A>C
NG_009775.2:g.67152A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.478-97A>C MANE Select	ENSP00000318351.5:n.478-97A>C
ENST00000320393.8:c.478-97A>C	ENSP00000318351.5:n.478-97A>C
ENST00000356489.9:c.478-97A>C	ENSP00000348880.5:n.478-97A>C
ENST00000369760.8:c.478-97A>C	ENSP00000358775.4:n.478-97A>C
NM_000056.3:c.478-97A>C	NP_000047.1:n.478-97A>C
NM_183050.2:c.478-97A>C	NP_898871.1:n.478-97A>C
XM_005248756.3:c.478-97A>C	XP_005248813.1:n.478-97A>C
XM_006715542.2:c.268-97A>C	XP_006715605.1:n.268-97A>C
XM_011536023.1:c.478-97A>C	XP_011534325.1:n.478-97A>C
XM_011536024.1:c.478-97A>C	XP_011534326.1:n.478-97A>C
XM_011536025.1:c.478-97A>C	XP_011534327.1:n.478-97A>C
XM_011536026.1:c.268-97A>C	XP_011534328.1:n.268-97A>C
XM_011536027.1:c.478-97A>C	XP_011534329.1:n.478-97A>C
NM_000056.4:c.478-97A>C	NP_000047.1:n.478-97A>C
NM_001318975.1:c.268-97A>C	NP_001305904.1:n.268-97A>C
NM_183050.3:c.478-97A>C	NP_898871.1:n.478-97A>C
NR_134945.1:n.562-97A>C
XM_005248756.5:c.478-97A>C	XP_005248813.1:n.478-97A>C
XM_011536023.3:c.478-97A>C	XP_011534325.1:n.478-97A>C
XM_011536024.3:c.478-97A>C	XP_011534326.1:n.478-97A>C
XM_011536025.3:c.478-97A>C	XP_011534327.1:n.478-97A>C
XR_001743546.2:n.508-97A>C
XR_001743547.2:n.508-97A>C
XR_001743548.2:n.508-97A>C
XR_001743549.2:n.508-97A>C
XR_002956292.1:n.508-97A>C
NM_183050.4:c.478-97A>C MANE Select	NP_898871.1:n.478-97A>C
NR_134945.2:n.501-97A>C
NM_000056.5:c.478-97A>C	NP_000047.1:n.478-97A>C