Canonical Allele Identifier: CA1239745858

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285523A= , CM000664.2:g.26285523A=	GRCh38
NC_000002.11:g.26508391A= , CM000664.1:g.26508391A=	GRCh37
NC_000002.10:g.26361895A=	NCBI36
NG_007294.1:g.45571A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317799.10:c.1341A= MANE Select	ENSP00000325136.5:p.Lys447=
ENST00000317799.9:c.1341A=	ENSP00000325136.5:p.Lys447=
ENST00000405867.7:c.972A=	ENSP00000385411.3:p.Lys324=
ENST00000494615.1:n.2288A=
ENST00000537713.5:c.1296A=	ENSP00000444295.1:p.Lys432=
ENST00000545822.2:c.1275A=	ENSP00000442665.1:p.Lys425=
NM_000183.2:c.1341A=	NP_000174.1:p.Lys447=
NM_001281512.1:c.1296A=	NP_001268441.1:p.Lys432=
NM_001281513.1:c.1275A=	NP_001268442.1:p.Lys425=
XM_011532803.1:c.1341A=	XP_011531105.1:p.Lys447=
XM_011532804.1:c.1275A=	XP_011531106.1:p.Lys425=
XM_024452830.1:c.1311A=	XP_024308598.1:p.Lys437=
XM_024452831.1:c.1275A=	XP_024308599.1:p.Lys425=
NM_000183.3:c.1341A= MANE Select	NP_000174.1:p.Lys447=
NM_001281513.2:c.1275A=	NP_001268442.1:p.Lys425=
NM_001281512.2:c.1296A=	NP_001268441.1:p.Lys432=