Canonical Allele Identifier: CA355113485
Gene: BCHE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830912A>T , CM000665.2:g.165830912A>T GRCh38
NC_000003.11:g.165548700A>T , CM000665.1:g.165548700A>T GRCh37
NC_000003.10:g.167031394A>T NCBI36
NG_009031.1:g.11554T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264381.8:c.122T>A MANE Select ENSP00000264381.3:p.Val41Asp
ENST00000264381.7:c.122T>A ENSP00000264381.3:p.Val41Asp
ENST00000479451.5:c.107+6402T>A ENSP00000418325.1:n.107+6402T>A
ENST00000482958.1:c.122T>A ENSP00000419804.1:p.Val41Asp
ENST00000488954.1:c.107+6402T>A ENSP00000418504.1:n.107+6402T>A
ENST00000497011.5:c.122T>A ENSP00000419505.1:p.Val41Asp
NM_000055.2:c.122T>A NP_000046.1:p.Val41Asp
XM_005247685.1:c.245T>A XP_005247742.1:p.Val82Asp
NM_000055.3:c.122T>A NP_000046.1:p.Val41Asp
NR_137635.1:n.159+6402T>A
NR_137636.1:n.289T>A
NM_000055.4:c.122T>A MANE Select NP_000046.1:p.Val41Asp
NR_137635.2:n.110+6402T>A
NR_137636.2:n.240T>A