Canonical Allele Identifier: CA1239731779

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26263382G= , CM000664.2:g.26263382G=	GRCh38
NC_000002.11:g.26486250G= , CM000664.1:g.26486250G=	GRCh37
NC_000002.10:g.26339754G=	NCBI36
NG_007294.1:g.23430G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.112G= MANE Select	ENSP00000325136.5:p.Val38=
ENST00000317799.9:c.112G=	ENSP00000325136.5:p.Val38=
ENST00000405867.7:c.112G=	ENSP00000385411.3:p.Val38=
ENST00000412805.5:c.112G=	ENSP00000413103.1:p.Val38=
ENST00000425035.5:c.112G=	ENSP00000404633.1:p.Val38=
ENST00000448743.5:c.112G=	ENSP00000415300.1:p.Val38=
ENST00000494615.1:n.1059G=
ENST00000537713.5:c.112G=	ENSP00000444295.1:p.Val38=
ENST00000545822.2:c.46G=	ENSP00000442665.1:p.Val16=
NM_000183.2:c.112G=	NP_000174.1:p.Val38=
NM_001281512.1:c.112G=	NP_001268441.1:p.Val38=
NM_001281513.1:c.46G=	NP_001268442.1:p.Val16=
XM_011532803.1:c.112G=	XP_011531105.1:p.Val38=
XM_011532804.1:c.46G=	XP_011531106.1:p.Val16=
XM_024452830.1:c.82G=	XP_024308598.1:p.Val28=
XM_024452831.1:c.46G=	XP_024308599.1:p.Val16=
NM_000183.3:c.112G= MANE Select	NP_000174.1:p.Val38=
NM_001281513.2:c.46G=	NP_001268442.1:p.Val16=
NM_001281512.2:c.112G=	NP_001268441.1:p.Val38=