Canonical Allele Identifier: CA355112088

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548041C>A (hg19) ; chr3:g.165830253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830253C>A , CM000665.2:g.165830253C>A	GRCh38
NC_000003.11:g.165548041C>A , CM000665.1:g.165548041C>A	GRCh37
NC_000003.10:g.167030735C>A	NCBI36
NG_009031.1:g.12213G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.781G>T MANE Select	ENSP00000264381.3:p.Val261Leu
ENST00000264381.7:c.781G>T	ENSP00000264381.3:p.Val261Leu
ENST00000479451.5:c.107+7061G>T	ENSP00000418325.1:n.107+7061G>T
ENST00000482958.1:c.781G>T	ENSP00000419804.1:p.Val261Leu
ENST00000488954.1:c.107+7061G>T	ENSP00000418504.1:n.107+7061G>T
ENST00000497011.5:c.781G>T	ENSP00000419505.1:p.Val261Leu
NM_000055.2:c.781G>T	NP_000046.1:p.Val261Leu
XM_005247685.1:c.904G>T	XP_005247742.1:p.Val302Leu
NM_000055.3:c.781G>T	NP_000046.1:p.Val261Leu
NR_137635.1:n.159+7061G>T
NR_137636.1:n.948G>T
NM_000055.4:c.781G>T MANE Select	NP_000046.1:p.Val261Leu
NR_137635.2:n.110+7061G>T
NR_137636.2:n.899G>T