Canonical Allele Identifier: CA1417758847

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829296A= , CM000665.2:g.165829296A=	GRCh38
NC_000003.11:g.165547084A= , CM000665.1:g.165547084A=	GRCh37
NC_000003.10:g.167029778A=	NCBI36
NG_009031.1:g.13170T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1517+221T= MANE Select	ENSP00000264381.3:n.1517+221T=
ENST00000264381.7:c.1517+221T=	ENSP00000264381.3:n.1517+221T=
ENST00000479451.5:c.107+8018T=	ENSP00000418325.1:n.107+8018T=
ENST00000482958.1:c.1517+221T=	ENSP00000419804.1:n.1517+221T=
ENST00000488954.1:c.107+8018T=	ENSP00000418504.1:n.107+8018T=
ENST00000497011.5:c.1517+221T=	ENSP00000419505.1:n.1517+221T=
NM_000055.2:c.1517+221T=	NP_000046.1:n.1517+221T=
XM_005247685.1:c.1640+221T=	XP_005247742.1:n.1640+221T=
NM_000055.3:c.1517+221T=	NP_000046.1:n.1517+221T=
NR_137635.1:n.159+8018T=
NR_137636.1:n.1684+221T=
NM_000055.4:c.1517+221T= MANE Select	NP_000046.1:n.1517+221T=
NR_137635.2:n.110+8018T=
NR_137636.2:n.1635+221T=