Canonical Allele Identifier: CA1417711652

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786222G= , CM000665.2:g.165786222G=	GRCh38
NC_000003.11:g.165504010G= , CM000665.1:g.165504010G=	GRCh37
NC_000003.10:g.166986704G=	NCBI36
NG_009031.1:g.56244C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1607C= MANE Select	ENSP00000264381.3:p.Thr536=
ENST00000264381.7:c.1607C=	ENSP00000264381.3:p.Thr536=
ENST00000479451.5:c.197C=	ENSP00000418325.1:p.Thr66=
ENST00000482958.1:c.*113C=	ENSP00000419804.1:n.*113C=
ENST00000488954.1:c.197C=	ENSP00000418504.1:p.Thr66=
ENST00000497011.5:c.1607C=	ENSP00000419505.1:p.Thr536=
NM_000055.2:c.1607C=	NP_000046.1:p.Thr536=
XM_005247685.1:c.1730C=	XP_005247742.1:p.Thr577=
NM_000055.3:c.1607C=	NP_000046.1:p.Thr536=
NR_137635.1:n.249C=
NR_137636.1:n.1774C=
NM_000055.4:c.1607C= MANE Select	NP_000046.1:p.Thr536=
NR_137635.2:n.200C=
NR_137636.2:n.1725C=