Canonical Allele Identifier: CA2668431190

Gene: BCHE

Linked Data

• gnomAD v4: 3-165786410-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786410T>A , CM000665.2:g.165786410T>A	GRCh38
NC_000003.11:g.165504198T>A , CM000665.1:g.165504198T>A	GRCh37
NC_000003.10:g.166986892T>A	NCBI36
NG_009031.1:g.56056A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1518-99A>T MANE Select	ENSP00000264381.3:n.1518-99A>T
ENST00000264381.7:c.1518-99A>T	ENSP00000264381.3:n.1518-99A>T
ENST00000479451.5:c.108-99A>T	ENSP00000418325.1:n.108-99A>T
ENST00000482958.1:c.*24-99A>T	ENSP00000419804.1:n.*24-99A>T
ENST00000488954.1:c.108-99A>T	ENSP00000418504.1:n.108-99A>T
ENST00000497011.5:c.1518-99A>T	ENSP00000419505.1:n.1518-99A>T
NM_000055.2:c.1518-99A>T	NP_000046.1:n.1518-99A>T
XM_005247685.1:c.1641-99A>T	XP_005247742.1:n.1641-99A>T
NM_000055.3:c.1518-99A>T	NP_000046.1:n.1518-99A>T
NR_137635.1:n.160-99A>T
NR_137636.1:n.1685-99A>T
NM_000055.4:c.1518-99A>T MANE Select	NP_000046.1:n.1518-99A>T
NR_137635.2:n.111-99A>T
NR_137636.2:n.1636-99A>T