Canonical Allele Identifier: CA1417760840
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830739G= , CM000665.2:g.165830739G= GRCh38
NC_000003.11:g.165548527G= , CM000665.1:g.165548527G= GRCh37
NC_000003.10:g.167031221G= NCBI36
NG_009031.1:g.11727C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.295C= MANE Select ENSP00000264381.3:p.Gln99=
ENST00000264381.7:c.295C= ENSP00000264381.3:p.Gln99=
ENST00000479451.5:c.107+6575C= ENSP00000418325.1:n.107+6575C=
ENST00000482958.1:c.295C= ENSP00000419804.1:p.Gln99=
ENST00000488954.1:c.107+6575C= ENSP00000418504.1:n.107+6575C=
ENST00000497011.5:c.295C= ENSP00000419505.1:p.Gln99=
NM_000055.2:c.295C= NP_000046.1:p.Gln99=
XM_005247685.1:c.418C= XP_005247742.1:p.Gln140=
NM_000055.3:c.295C= NP_000046.1:p.Gln99=
NR_137635.1:n.159+6575C=
NR_137636.1:n.462C=
NM_000055.4:c.295C= MANE Select NP_000046.1:p.Gln99=
NR_137635.2:n.110+6575C=
NR_137636.2:n.413C=