Canonical Allele Identifier: CA1239745835

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285476G= , CM000664.2:g.26285476G=	GRCh38
NC_000002.11:g.26508344G= , CM000664.1:g.26508344G=	GRCh37
NC_000002.10:g.26361848G=	NCBI36
NG_007294.1:g.45524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1294G= MANE Select	ENSP00000325136.5:p.Ala432=
ENST00000317799.9:c.1294G=	ENSP00000325136.5:p.Ala432=
ENST00000405867.7:c.925G=	ENSP00000385411.3:p.Ala309=
ENST00000494615.1:n.2241G=
ENST00000537713.5:c.1249G=	ENSP00000444295.1:p.Ala417=
ENST00000545822.2:c.1228G=	ENSP00000442665.1:p.Ala410=
NM_000183.2:c.1294G=	NP_000174.1:p.Ala432=
NM_001281512.1:c.1249G=	NP_001268441.1:p.Ala417=
NM_001281513.1:c.1228G=	NP_001268442.1:p.Ala410=
XM_011532803.1:c.1294G=	XP_011531105.1:p.Ala432=
XM_011532804.1:c.1228G=	XP_011531106.1:p.Ala410=
XM_024452830.1:c.1264G=	XP_024308598.1:p.Ala422=
XM_024452831.1:c.1228G=	XP_024308599.1:p.Ala410=
NM_000183.3:c.1294G= MANE Select	NP_000174.1:p.Ala432=
NM_001281513.2:c.1228G=	NP_001268442.1:p.Ala410=
NM_001281512.2:c.1249G=	NP_001268441.1:p.Ala417=