Canonical Allele Identifier: CA1417760127
Gene: BCHE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830197A= , CM000665.2:g.165830197A= GRCh38
NC_000003.11:g.165547985A= , CM000665.1:g.165547985A= GRCh37
NC_000003.10:g.167030679A= NCBI36
NG_009031.1:g.12269T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.837T= MANE Select ENSP00000264381.3:p.Gly279=
ENST00000264381.7:c.837T= ENSP00000264381.3:p.Gly279=
ENST00000479451.5:c.107+7117T= ENSP00000418325.1:n.107+7117T=
ENST00000482958.1:c.837T= ENSP00000419804.1:p.Gly279=
ENST00000488954.1:c.107+7117T= ENSP00000418504.1:n.107+7117T=
ENST00000497011.5:c.837T= ENSP00000419505.1:p.Gly279=
NM_000055.2:c.837T= NP_000046.1:p.Gly279=
XM_005247685.1:c.960T= XP_005247742.1:p.Gly320=
NM_000055.3:c.837T= NP_000046.1:p.Gly279=
NR_137635.1:n.159+7117T=
NR_137636.1:n.1004T=
NM_000055.4:c.837T= MANE Select NP_000046.1:p.Gly279=
NR_137635.2:n.110+7117T=
NR_137636.2:n.955T=