Canonical Allele Identifier: CA355111201

Gene: BCHE

Linked Data

• gnomAD v4: 3-165829845-T-C
• MyVariant Identifiers: chr3:g.165547633T>C (hg19) ; chr3:g.165829845T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829845T>C , CM000665.2:g.165829845T>C	GRCh38
NC_000003.11:g.165547633T>C , CM000665.1:g.165547633T>C	GRCh37
NC_000003.10:g.167030327T>C	NCBI36
NG_009031.1:g.12621A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1189A>G MANE Select	ENSP00000264381.3:p.Ile397Val
ENST00000264381.7:c.1189A>G	ENSP00000264381.3:p.Ile397Val
ENST00000479451.5:c.107+7469A>G	ENSP00000418325.1:n.107+7469A>G
ENST00000482958.1:c.1189A>G	ENSP00000419804.1:p.Ile397Val
ENST00000488954.1:c.107+7469A>G	ENSP00000418504.1:n.107+7469A>G
ENST00000497011.5:c.1189A>G	ENSP00000419505.1:p.Ile397Val
NM_000055.2:c.1189A>G	NP_000046.1:p.Ile397Val
XM_005247685.1:c.1312A>G	XP_005247742.1:p.Ile438Val
NM_000055.3:c.1189A>G	NP_000046.1:p.Ile397Val
NR_137635.1:n.159+7469A>G
NR_137636.1:n.1356A>G
NM_000055.4:c.1189A>G MANE Select	NP_000046.1:p.Ile397Val
NR_137635.2:n.110+7469A>G
NR_137636.2:n.1307A>G