Canonical Allele Identifier: CA1417760871
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830827A= , CM000665.2:g.165830827A= GRCh38
NC_000003.11:g.165548615A= , CM000665.1:g.165548615A= GRCh37
NC_000003.10:g.167031309A= NCBI36
NG_009031.1:g.11639T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.207T= MANE Select ENSP00000264381.3:p.Leu69=
ENST00000264381.7:c.207T= ENSP00000264381.3:p.Leu69=
ENST00000479451.5:c.107+6487T= ENSP00000418325.1:n.107+6487T=
ENST00000482958.1:c.207T= ENSP00000419804.1:p.Leu69=
ENST00000488954.1:c.107+6487T= ENSP00000418504.1:n.107+6487T=
ENST00000497011.5:c.207T= ENSP00000419505.1:p.Leu69=
NM_000055.2:c.207T= NP_000046.1:p.Leu69=
XM_005247685.1:c.330T= XP_005247742.1:p.Leu110=
NM_000055.3:c.207T= NP_000046.1:p.Leu69=
NR_137635.1:n.159+6487T=
NR_137636.1:n.374T=
NM_000055.4:c.207T= MANE Select NP_000046.1:p.Leu69=
NR_137635.2:n.110+6487T=
NR_137636.2:n.325T=