Canonical Allele Identifier: CA1239731778

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26263381T= , CM000664.2:g.26263381T=	GRCh38
NC_000002.11:g.26486249T= , CM000664.1:g.26486249T=	GRCh37
NC_000002.10:g.26339753T=	NCBI36
NG_007294.1:g.23429T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.111T= MANE Select	ENSP00000325136.5:p.Ala37=
ENST00000317799.9:c.111T=	ENSP00000325136.5:p.Ala37=
ENST00000405867.7:c.111T=	ENSP00000385411.3:p.Ala37=
ENST00000412805.5:c.111T=	ENSP00000413103.1:p.Ala37=
ENST00000425035.5:c.111T=	ENSP00000404633.1:p.Ala37=
ENST00000448743.5:c.111T=	ENSP00000415300.1:p.Ala37=
ENST00000494615.1:n.1058T=
ENST00000537713.5:c.111T=	ENSP00000444295.1:p.Ala37=
ENST00000545822.2:c.45T=	ENSP00000442665.1:p.Ala15=
NM_000183.2:c.111T=	NP_000174.1:p.Ala37=
NM_001281512.1:c.111T=	NP_001268441.1:p.Ala37=
NM_001281513.1:c.45T=	NP_001268442.1:p.Ala15=
XM_011532803.1:c.111T=	XP_011531105.1:p.Ala37=
XM_011532804.1:c.45T=	XP_011531106.1:p.Ala15=
XM_024452830.1:c.81T=	XP_024308598.1:p.Ala27=
XM_024452831.1:c.45T=	XP_024308599.1:p.Ala15=
NM_000183.3:c.111T= MANE Select	NP_000174.1:p.Ala37=
NM_001281513.2:c.45T=	NP_001268442.1:p.Ala15=
NM_001281512.2:c.111T=	NP_001268441.1:p.Ala37=