Canonical Allele Identifier: CA355113337

Gene: BCHE

Linked Data

• COSMIC: COSM729276
• MyVariant Identifiers: chr3:g.165548626G>T (hg19) ; chr3:g.165830838G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830838G>T , CM000665.2:g.165830838G>T	GRCh38
NC_000003.11:g.165548626G>T , CM000665.1:g.165548626G>T	GRCh37
NC_000003.10:g.167031320G>T	NCBI36
NG_009031.1:g.11628C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.196C>A MANE Select	ENSP00000264381.3:p.Leu66Ile
ENST00000264381.7:c.196C>A	ENSP00000264381.3:p.Leu66Ile
ENST00000479451.5:c.107+6476C>A	ENSP00000418325.1:n.107+6476C>A
ENST00000482958.1:c.196C>A	ENSP00000419804.1:p.Leu66Ile
ENST00000488954.1:c.107+6476C>A	ENSP00000418504.1:n.107+6476C>A
ENST00000497011.5:c.196C>A	ENSP00000419505.1:p.Leu66Ile
NM_000055.2:c.196C>A	NP_000046.1:p.Leu66Ile
XM_005247685.1:c.319C>A	XP_005247742.1:p.Leu107Ile
NM_000055.3:c.196C>A	NP_000046.1:p.Leu66Ile
NR_137635.1:n.159+6476C>A
NR_137636.1:n.363C>A
NM_000055.4:c.196C>A MANE Select	NP_000046.1:p.Leu66Ile
NR_137635.2:n.110+6476C>A
NR_137636.2:n.314C>A