Canonical Allele Identifier: CA355110783

Gene: BCHE

Linked Data

• gnomAD v4: 3-165829658-G-A
• MyVariant Identifiers: chr3:g.165547446G>A (hg19) ; chr3:g.165829658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829658G>A , CM000665.2:g.165829658G>A	GRCh38
NC_000003.11:g.165547446G>A , CM000665.1:g.165547446G>A	GRCh37
NC_000003.10:g.167030140G>A	NCBI36
NG_009031.1:g.12808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1376C>T MANE Select	ENSP00000264381.3:p.Pro459Leu
ENST00000264381.7:c.1376C>T	ENSP00000264381.3:p.Pro459Leu
ENST00000479451.5:c.107+7656C>T	ENSP00000418325.1:n.107+7656C>T
ENST00000482958.1:c.1376C>T	ENSP00000419804.1:p.Pro459Leu
ENST00000488954.1:c.107+7656C>T	ENSP00000418504.1:n.107+7656C>T
ENST00000497011.5:c.1376C>T	ENSP00000419505.1:p.Pro459Leu
NM_000055.2:c.1376C>T	NP_000046.1:p.Pro459Leu
XM_005247685.1:c.1499C>T	XP_005247742.1:p.Pro500Leu
NM_000055.3:c.1376C>T	NP_000046.1:p.Pro459Leu
NR_137635.1:n.159+7656C>T
NR_137636.1:n.1543C>T
NM_000055.4:c.1376C>T MANE Select	NP_000046.1:p.Pro459Leu
NR_137635.2:n.110+7656C>T
NR_137636.2:n.1494C>T