Canonical Allele Identifier: CA1417698897

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773568T= , CM000665.2:g.165773568T=	GRCh38
NC_000003.11:g.165491356T= , CM000665.1:g.165491356T=	GRCh37
NC_000003.10:g.166974050T=	NCBI36
NG_009031.1:g.68898A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1685-62A= MANE Select	ENSP00000264381.3:n.1685-62A=
ENST00000264381.7:c.1685-62A=	ENSP00000264381.3:n.1685-62A=
ENST00000479451.5:c.275-62A=	ENSP00000418325.1:n.275-62A=
ENST00000482958.1:c.*191-62A=	ENSP00000419804.1:n.*191-62A=
ENST00000497011.5:c.*75-62A=	ENSP00000419505.1:n.*75-62A=
NM_000055.2:c.1685-62A=	NP_000046.1:n.1685-62A=
XM_005247685.1:c.1808-62A=	XP_005247742.1:n.1808-62A=
NM_000055.3:c.1685-62A=	NP_000046.1:n.1685-62A=
NR_137635.1:n.327-62A=
NR_137636.1:n.1931-62A=
NM_000055.4:c.1685-62A= MANE Select	NP_000046.1:n.1685-62A=
NR_137635.2:n.278-62A=
NR_137636.2:n.1882-62A=