Canonical Allele Identifier: CA2668431229

Gene: BCHE

Linked Data

• gnomAD v4: 3-165786463-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786463G>T , CM000665.2:g.165786463G>T	GRCh38
NC_000003.11:g.165504251G>T , CM000665.1:g.165504251G>T	GRCh37
NC_000003.10:g.166986945G>T	NCBI36
NG_009031.1:g.56003C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1518-152C>A MANE Select	ENSP00000264381.3:n.1518-152C>A
ENST00000264381.7:c.1518-152C>A	ENSP00000264381.3:n.1518-152C>A
ENST00000479451.5:c.108-152C>A	ENSP00000418325.1:n.108-152C>A
ENST00000482958.1:c.*24-152C>A	ENSP00000419804.1:n.*24-152C>A
ENST00000488954.1:c.108-152C>A	ENSP00000418504.1:n.108-152C>A
ENST00000497011.5:c.1518-152C>A	ENSP00000419505.1:n.1518-152C>A
NM_000055.2:c.1518-152C>A	NP_000046.1:n.1518-152C>A
XM_005247685.1:c.1641-152C>A	XP_005247742.1:n.1641-152C>A
NM_000055.3:c.1518-152C>A	NP_000046.1:n.1518-152C>A
NR_137635.1:n.160-152C>A
NR_137636.1:n.1685-152C>A
NM_000055.4:c.1518-152C>A MANE Select	NP_000046.1:n.1518-152C>A
NR_137635.2:n.111-152C>A
NR_137636.2:n.1636-152C>A