Canonical Allele Identifier: CA355112169

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548079G>T (hg19) ; chr3:g.165830291G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830291G>T , CM000665.2:g.165830291G>T	GRCh38
NC_000003.11:g.165548079G>T , CM000665.1:g.165548079G>T	GRCh37
NC_000003.10:g.167030773G>T	NCBI36
NG_009031.1:g.12175C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.743C>A MANE Select	ENSP00000264381.3:p.Ala248Asp
ENST00000264381.7:c.743C>A	ENSP00000264381.3:p.Ala248Asp
ENST00000479451.5:c.107+7023C>A	ENSP00000418325.1:n.107+7023C>A
ENST00000482958.1:c.743C>A	ENSP00000419804.1:p.Ala248Asp
ENST00000488954.1:c.107+7023C>A	ENSP00000418504.1:n.107+7023C>A
ENST00000497011.5:c.743C>A	ENSP00000419505.1:p.Ala248Asp
NM_000055.2:c.743C>A	NP_000046.1:p.Ala248Asp
XM_005247685.1:c.866C>A	XP_005247742.1:p.Ala289Asp
NM_000055.3:c.743C>A	NP_000046.1:p.Ala248Asp
NR_137635.1:n.159+7023C>A
NR_137636.1:n.910C>A
NM_000055.4:c.743C>A MANE Select	NP_000046.1:p.Ala248Asp
NR_137635.2:n.110+7023C>A
NR_137636.2:n.861C>A