Canonical Allele Identifier: CA355111632
Gene: BCHE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165830039T>G , CM000665.2:g.165830039T>G GRCh38
NC_000003.11:g.165547827T>G , CM000665.1:g.165547827T>G GRCh37
NC_000003.10:g.167030521T>G NCBI36
NG_009031.1:g.12427A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264381.8:c.995A>C MANE Select ENSP00000264381.3:p.Asp332Ala
ENST00000264381.7:c.995A>C ENSP00000264381.3:p.Asp332Ala
ENST00000479451.5:c.107+7275A>C ENSP00000418325.1:n.107+7275A>C
ENST00000482958.1:c.995A>C ENSP00000419804.1:p.Asp332Ala
ENST00000488954.1:c.107+7275A>C ENSP00000418504.1:n.107+7275A>C
ENST00000497011.5:c.995A>C ENSP00000419505.1:p.Asp332Ala
NM_000055.2:c.995A>C NP_000046.1:p.Asp332Ala
XM_005247685.1:c.1118A>C XP_005247742.1:p.Asp373Ala
NM_000055.3:c.995A>C NP_000046.1:p.Asp332Ala
NR_137635.1:n.159+7275A>C
NR_137636.1:n.1162A>C
NM_000055.4:c.995A>C MANE Select NP_000046.1:p.Asp332Ala
NR_137635.2:n.110+7275A>C
NR_137636.2:n.1113A>C