Canonical Allele Identifier: CA1417711623

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786201C= , CM000665.2:g.165786201C=	GRCh38
NC_000003.11:g.165503989C= , CM000665.1:g.165503989C=	GRCh37
NC_000003.10:g.166986683C=	NCBI36
NG_009031.1:g.56265G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1628G= MANE Select	ENSP00000264381.3:p.Arg543=
ENST00000264381.7:c.1628G=	ENSP00000264381.3:p.Arg543=
ENST00000479451.5:c.218G=	ENSP00000418325.1:p.Arg73=
ENST00000482958.1:c.*134G=	ENSP00000419804.1:n.*134G=
ENST00000488954.1:c.218G=	ENSP00000418504.1:p.Arg73=
ENST00000497011.5:c.1628G=	ENSP00000419505.1:p.Arg543=
NM_000055.2:c.1628G=	NP_000046.1:p.Arg543=
XM_005247685.1:c.1751G=	XP_005247742.1:p.Arg584=
NM_000055.3:c.1628G=	NP_000046.1:p.Arg543=
NR_137635.1:n.270G=
NR_137636.1:n.1795G=
NM_000055.4:c.1628G= MANE Select	NP_000046.1:p.Arg543=
NR_137635.2:n.221G=
NR_137636.2:n.1746G=