Canonical Allele Identifier: CA1417713581
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165788106C= , CM000665.2:g.165788106C= GRCh38
NC_000003.11:g.165505894C= , CM000665.1:g.165505894C= GRCh37
NC_000003.10:g.166988588C= NCBI36
NG_009031.1:g.54360G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.1518-1795G= MANE Select ENSP00000264381.3:n.1518-1795G=
ENST00000264381.7:c.1518-1795G= ENSP00000264381.3:n.1518-1795G=
ENST00000479451.5:c.108-1795G= ENSP00000418325.1:n.108-1795G=
ENST00000482958.1:c.*24-1795G= ENSP00000419804.1:n.*24-1795G=
ENST00000488954.1:c.108-1795G= ENSP00000418504.1:n.108-1795G=
ENST00000497011.5:c.1518-1795G= ENSP00000419505.1:n.1518-1795G=
NM_000055.2:c.1518-1795G= NP_000046.1:n.1518-1795G=
XM_005247685.1:c.1641-1795G= XP_005247742.1:n.1641-1795G=
NM_000055.3:c.1518-1795G= NP_000046.1:n.1518-1795G=
NR_137635.1:n.160-1795G=
NR_137636.1:n.1685-1795G=
NM_000055.4:c.1518-1795G= MANE Select NP_000046.1:n.1518-1795G=
NR_137635.2:n.111-1795G=
NR_137636.2:n.1636-1795G=