Canonical Allele Identifier: CA2692358
Gene: BCHE HGNC NCBI

Linked Data

dbSNP Id: rs747438953

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165829856C>T , CM000665.2:g.165829856C>T GRCh38
NC_000003.11:g.165547644C>T , CM000665.1:g.165547644C>T GRCh37
NC_000003.10:g.167030338C>T NCBI36
NG_009031.1:g.12610G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.1178G>A MANE Select ENSP00000264381.3:p.Gly393Glu
ENST00000264381.7:c.1178G>A ENSP00000264381.3:p.Gly393Glu
ENST00000479451.5:c.107+7458G>A ENSP00000418325.1:n.107+7458G>A
ENST00000482958.1:c.1178G>A ENSP00000419804.1:p.Gly393Glu
ENST00000488954.1:c.107+7458G>A ENSP00000418504.1:n.107+7458G>A
ENST00000497011.5:c.1178G>A ENSP00000419505.1:p.Gly393Glu
NM_000055.2:c.1178G>A NP_000046.1:p.Gly393Glu
XM_005247685.1:c.1301G>A XP_005247742.1:p.Gly434Glu
NM_000055.3:c.1178G>A NP_000046.1:p.Gly393Glu
NR_137635.1:n.159+7458G>A
NR_137636.1:n.1345G>A
NM_000055.4:c.1178G>A MANE Select NP_000046.1:p.Gly393Glu
NR_137635.2:n.110+7458G>A
NR_137636.2:n.1296G>A