Canonical Allele Identifier: CA3108891902
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830127T= , CM000665.2:g.165830127T= GRCh38
NC_000003.11:g.165547915T= , CM000665.1:g.165547915T= GRCh37
NC_000003.10:g.167030609T= NCBI36
NG_009031.1:g.12339A=

Transcript Alleles

HGVS Amino-acid Change
NM_000055.4:c.907A= MANE Select NP_000046.1:p.Asn303=
ENST00000264381.8:c.907A= MANE Select ENSP00000264381.3:p.Asn303=
NM_000055.2:c.907A= NP_000046.1:p.Asn303=
NM_000055.3:c.907A= NP_000046.1:p.Asn303=
NR_137635.1:n.159+7187A=
NR_137635.2:n.110+7187A=
NR_137636.1:n.1074A=
NR_137636.2:n.1025A=
ENST00000264381.7:c.907A= ENSP00000264381.3:p.Asn303=
ENST00000479451.5:c.107+7187A= ENSP00000418325.1:n.107+7187A=
ENST00000482958.1:c.907A= ENSP00000419804.1:p.Asn303=
ENST00000488954.1:c.107+7187A= ENSP00000418504.1:n.107+7187A=
ENST00000497011.5:c.907A= ENSP00000419505.1:p.Asn303=
XM_005247685.1:c.1030A= XP_005247742.1:p.Asn344=