Canonical Allele Identifier: CA355110091

Gene: BCHE

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786144C>T , CM000665.2:g.165786144C>T	GRCh38
NC_000003.11:g.165503932C>T , CM000665.1:g.165503932C>T	GRCh37
NC_000003.10:g.166986626C>T	NCBI36
NG_009031.1:g.56322G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1684+1G>A MANE Select	ENSP00000264381.3:n.1684+1G>A
ENST00000264381.7:c.1684+1G>A	ENSP00000264381.3:n.1684+1G>A
ENST00000479451.5:c.274+1G>A	ENSP00000418325.1:n.274+1G>A
ENST00000482958.1:c.*190+1G>A	ENSP00000419804.1:n.*190+1G>A
ENST00000488954.1:c.274+1G>A	ENSP00000418504.1:n.274+1G>A
ENST00000497011.5:c.1684+1G>A	ENSP00000419505.1:n.1684+1G>A
NM_000055.2:c.1684+1G>A	NP_000046.1:n.1684+1G>A
XM_005247685.1:c.1807+1G>A	XP_005247742.1:n.1807+1G>A
NM_000055.3:c.1684+1G>A	NP_000046.1:n.1684+1G>A
NR_137635.1:n.326+1G>A
NR_137636.1:n.1851+1G>A
NM_000055.4:c.1684+1G>A MANE Select	NP_000046.1:n.1684+1G>A
NR_137635.2:n.277+1G>A
NR_137636.2:n.1802+1G>A