Canonical Allele Identifier: CA1239731833

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26263501T= , CM000664.2:g.26263501T=	GRCh38
NC_000002.11:g.26486369T= , CM000664.1:g.26486369T=	GRCh37
NC_000002.10:g.26339873T=	NCBI36
NG_007294.1:g.23549T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.209+22T= MANE Select	ENSP00000325136.5:n.209+22T=
ENST00000317799.9:c.209+22T=	ENSP00000325136.5:n.209+22T=
ENST00000405867.7:c.209+22T=	ENSP00000385411.3:n.209+22T=
ENST00000412805.5:c.209+22T=	ENSP00000413103.1:n.209+22T=
ENST00000425035.5:c.209+22T=	ENSP00000404633.1:n.209+22T=
ENST00000448743.5:c.209+22T=	ENSP00000415300.1:n.209+22T=
ENST00000494615.1:n.1156+22T=
ENST00000537713.5:c.209+22T=	ENSP00000444295.1:n.209+22T=
ENST00000545822.2:c.143+22T=	ENSP00000442665.1:n.143+22T=
NM_000183.2:c.209+22T=	NP_000174.1:n.209+22T=
NM_001281512.1:c.209+22T=	NP_001268441.1:n.209+22T=
NM_001281513.1:c.143+22T=	NP_001268442.1:n.143+22T=
XM_011532803.1:c.209+22T=	XP_011531105.1:n.209+22T=
XM_011532804.1:c.143+22T=	XP_011531106.1:n.143+22T=
XM_024452830.1:c.179+22T=	XP_024308598.1:n.179+22T=
XM_024452831.1:c.143+22T=	XP_024308599.1:n.143+22T=
NM_000183.3:c.209+22T= MANE Select	NP_000174.1:n.209+22T=
NM_001281513.2:c.143+22T=	NP_001268442.1:n.143+22T=
NM_001281512.2:c.209+22T=	NP_001268441.1:n.209+22T=