Canonical Allele Identifier: CA1417758922

Gene: BCHE

Linked Data

• dbSNP Id: rs1714857099
• gnomAD v4: 3-165829369-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829375dup , CM000665.2:g.165829375dup	GRCh38
NC_000003.11:g.165547163dup , CM000665.1:g.165547163dup	GRCh37
NC_000003.10:g.167029857dup	NCBI36
NG_009031.1:g.13096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1517+147dup MANE Select	ENSP00000264381.3:n.1517+147dup
ENST00000264381.7:c.1517+147dup	ENSP00000264381.3:n.1517+147dup
ENST00000479451.5:c.107+7944dup	ENSP00000418325.1:n.107+7944dup
ENST00000482958.1:c.1517+147dup	ENSP00000419804.1:n.1517+147dup
ENST00000488954.1:c.107+7944dup	ENSP00000418504.1:n.107+7944dup
ENST00000497011.5:c.1517+147dup	ENSP00000419505.1:n.1517+147dup
NM_000055.2:c.1517+147dup	NP_000046.1:n.1517+147dup
XM_005247685.1:c.1640+147dup	XP_005247742.1:n.1640+147dup
NM_000055.3:c.1517+147dup	NP_000046.1:n.1517+147dup
NR_137635.1:n.159+7944dup
NR_137636.1:n.1684+147dup
NM_000055.4:c.1517+147dup MANE Select	NP_000046.1:n.1517+147dup
NR_137635.2:n.110+7944dup
NR_137636.2:n.1635+147dup