Canonical Allele Identifier: CA1417759398
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165829706T= , CM000665.2:g.165829706T= GRCh38
NC_000003.11:g.165547494T= , CM000665.1:g.165547494T= GRCh37
NC_000003.10:g.167030188T= NCBI36
NG_009031.1:g.12760A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.1328A= MANE Select ENSP00000264381.3:p.Asn443=
ENST00000264381.7:c.1328A= ENSP00000264381.3:p.Asn443=
ENST00000479451.5:c.107+7608A= ENSP00000418325.1:n.107+7608A=
ENST00000482958.1:c.1328A= ENSP00000419804.1:p.Asn443=
ENST00000488954.1:c.107+7608A= ENSP00000418504.1:n.107+7608A=
ENST00000497011.5:c.1328A= ENSP00000419505.1:p.Asn443=
NM_000055.2:c.1328A= NP_000046.1:p.Asn443=
XM_005247685.1:c.1451A= XP_005247742.1:p.Asn484=
NM_000055.3:c.1328A= NP_000046.1:p.Asn443=
NR_137635.1:n.159+7608A=
NR_137636.1:n.1495A=
NM_000055.4:c.1328A= MANE Select NP_000046.1:p.Asn443=
NR_137635.2:n.110+7608A=
NR_137636.2:n.1446A=