Canonical Allele Identifier: CA1417760752

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830567T= , CM000665.2:g.165830567T=	GRCh38
NC_000003.11:g.165548355T= , CM000665.1:g.165548355T=	GRCh37
NC_000003.10:g.167031049T=	NCBI36
NG_009031.1:g.11899A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.467A= MANE Select	ENSP00000264381.3:p.Tyr156=
ENST00000264381.7:c.467A=	ENSP00000264381.3:p.Tyr156=
ENST00000479451.5:c.107+6747A=	ENSP00000418325.1:n.107+6747A=
ENST00000482958.1:c.467A=	ENSP00000419804.1:p.Tyr156=
ENST00000488954.1:c.107+6747A=	ENSP00000418504.1:n.107+6747A=
ENST00000497011.5:c.467A=	ENSP00000419505.1:p.Tyr156=
NM_000055.2:c.467A=	NP_000046.1:p.Tyr156=
XM_005247685.1:c.590A=	XP_005247742.1:p.Tyr197=
NM_000055.3:c.467A=	NP_000046.1:p.Tyr156=
NR_137635.1:n.159+6747A=
NR_137636.1:n.634A=
NM_000055.4:c.467A= MANE Select	NP_000046.1:p.Tyr156=
NR_137635.2:n.110+6747A=
NR_137636.2:n.585A=