Canonical Allele Identifier: CA1417760843
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830745T= , CM000665.2:g.165830745T= GRCh38
NC_000003.11:g.165548533T= , CM000665.1:g.165548533T= GRCh37
NC_000003.10:g.167031227T= NCBI36
NG_009031.1:g.11721A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.289A= MANE Select ENSP00000264381.3:p.Ile97=
ENST00000264381.7:c.289A= ENSP00000264381.3:p.Ile97=
ENST00000479451.5:c.107+6569A= ENSP00000418325.1:n.107+6569A=
ENST00000482958.1:c.289A= ENSP00000419804.1:p.Ile97=
ENST00000488954.1:c.107+6569A= ENSP00000418504.1:n.107+6569A=
ENST00000497011.5:c.289A= ENSP00000419505.1:p.Ile97=
NM_000055.2:c.289A= NP_000046.1:p.Ile97=
XM_005247685.1:c.412A= XP_005247742.1:p.Ile138=
NM_000055.3:c.289A= NP_000046.1:p.Ile97=
NR_137635.1:n.159+6569A=
NR_137636.1:n.456A=
NM_000055.4:c.289A= MANE Select NP_000046.1:p.Ile97=
NR_137635.2:n.110+6569A=
NR_137636.2:n.407A=