Canonical Allele Identifier: CA1239745819

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285417C= , CM000664.2:g.26285417C=	GRCh38
NC_000002.11:g.26508285C= , CM000664.1:g.26508285C=	GRCh37
NC_000002.10:g.26361789C=	NCBI36
NG_007294.1:g.45465C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1235C= MANE Select	ENSP00000325136.5:p.Pro412=
ENST00000317799.9:c.1235C=	ENSP00000325136.5:p.Pro412=
ENST00000405867.7:c.866C=	ENSP00000385411.3:p.Pro289=
ENST00000494615.1:n.2182C=
ENST00000537713.5:c.1190C=	ENSP00000444295.1:p.Pro397=
ENST00000545822.2:c.1169C=	ENSP00000442665.1:p.Pro390=
NM_000183.2:c.1235C=	NP_000174.1:p.Pro412=
NM_001281512.1:c.1190C=	NP_001268441.1:p.Pro397=
NM_001281513.1:c.1169C=	NP_001268442.1:p.Pro390=
XM_011532803.1:c.1235C=	XP_011531105.1:p.Pro412=
XM_011532804.1:c.1169C=	XP_011531106.1:p.Pro390=
XM_024452830.1:c.1205C=	XP_024308598.1:p.Pro402=
XM_024452831.1:c.1169C=	XP_024308599.1:p.Pro390=
NM_000183.3:c.1235C= MANE Select	NP_000174.1:p.Pro412=
NM_001281513.2:c.1169C=	NP_001268442.1:p.Pro390=
NM_001281512.2:c.1190C=	NP_001268441.1:p.Pro397=