Canonical Allele Identifier: CA355112131

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548061G>T (hg19) ; chr3:g.165830273G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830273G>T , CM000665.2:g.165830273G>T	GRCh38
NC_000003.11:g.165548061G>T , CM000665.1:g.165548061G>T	GRCh37
NC_000003.10:g.167030755G>T	NCBI36
NG_009031.1:g.12193C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.761C>A MANE Select	ENSP00000264381.3:p.Ser254Tyr
ENST00000264381.7:c.761C>A	ENSP00000264381.3:p.Ser254Tyr
ENST00000479451.5:c.107+7041C>A	ENSP00000418325.1:n.107+7041C>A
ENST00000482958.1:c.761C>A	ENSP00000419804.1:p.Ser254Tyr
ENST00000488954.1:c.107+7041C>A	ENSP00000418504.1:n.107+7041C>A
ENST00000497011.5:c.761C>A	ENSP00000419505.1:p.Ser254Tyr
NM_000055.2:c.761C>A	NP_000046.1:p.Ser254Tyr
XM_005247685.1:c.884C>A	XP_005247742.1:p.Ser295Tyr
NM_000055.3:c.761C>A	NP_000046.1:p.Ser254Tyr
NR_137635.1:n.159+7041C>A
NR_137636.1:n.928C>A
NM_000055.4:c.761C>A MANE Select	NP_000046.1:p.Ser254Tyr
NR_137635.2:n.110+7041C>A
NR_137636.2:n.879C>A