Canonical Allele Identifier: CA355113436

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548677A>T (hg19) ; chr3:g.165830889A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830889A>T , CM000665.2:g.165830889A>T	GRCh38
NC_000003.11:g.165548677A>T , CM000665.1:g.165548677A>T	GRCh37
NC_000003.10:g.167031371A>T	NCBI36
NG_009031.1:g.11577T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.145T>A MANE Select	ENSP00000264381.3:p.Phe49Ile
ENST00000264381.7:c.145T>A	ENSP00000264381.3:p.Phe49Ile
ENST00000479451.5:c.107+6425T>A	ENSP00000418325.1:n.107+6425T>A
ENST00000482958.1:c.145T>A	ENSP00000419804.1:p.Phe49Ile
ENST00000488954.1:c.107+6425T>A	ENSP00000418504.1:n.107+6425T>A
ENST00000497011.5:c.145T>A	ENSP00000419505.1:p.Phe49Ile
NM_000055.2:c.145T>A	NP_000046.1:p.Phe49Ile
XM_005247685.1:c.268T>A	XP_005247742.1:p.Phe90Ile
NM_000055.3:c.145T>A	NP_000046.1:p.Phe49Ile
NR_137635.1:n.159+6425T>A
NR_137636.1:n.312T>A
NM_000055.4:c.145T>A MANE Select	NP_000046.1:p.Phe49Ile
NR_137635.2:n.110+6425T>A
NR_137636.2:n.263T>A