Canonical Allele Identifier: CA1417711669

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786240G= , CM000665.2:g.165786240G=	GRCh38
NC_000003.11:g.165504028G= , CM000665.1:g.165504028G=	GRCh37
NC_000003.10:g.166986722G=	NCBI36
NG_009031.1:g.56226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1589C= MANE Select	ENSP00000264381.3:p.Thr530=
ENST00000264381.7:c.1589C=	ENSP00000264381.3:p.Thr530=
ENST00000479451.5:c.179C=	ENSP00000418325.1:p.Thr60=
ENST00000482958.1:c.*95C=	ENSP00000419804.1:n.*95C=
ENST00000488954.1:c.179C=	ENSP00000418504.1:p.Thr60=
ENST00000497011.5:c.1589C=	ENSP00000419505.1:p.Thr530=
NM_000055.2:c.1589C=	NP_000046.1:p.Thr530=
XM_005247685.1:c.1712C=	XP_005247742.1:p.Thr571=
NM_000055.3:c.1589C=	NP_000046.1:p.Thr530=
NR_137635.1:n.231C=
NR_137636.1:n.1756C=
NM_000055.4:c.1589C= MANE Select	NP_000046.1:p.Thr530=
NR_137635.2:n.182C=
NR_137636.2:n.1707C=