Canonical Allele Identifier: CA355111376

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165547710C>G (hg19) ; chr3:g.165829922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829922C>G , CM000665.2:g.165829922C>G	GRCh38
NC_000003.11:g.165547710C>G , CM000665.1:g.165547710C>G	GRCh37
NC_000003.10:g.167030404C>G	NCBI36
NG_009031.1:g.12544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1112G>C MANE Select	ENSP00000264381.3:p.Ser371Thr
ENST00000264381.7:c.1112G>C	ENSP00000264381.3:p.Ser371Thr
ENST00000479451.5:c.107+7392G>C	ENSP00000418325.1:n.107+7392G>C
ENST00000482958.1:c.1112G>C	ENSP00000419804.1:p.Ser371Thr
ENST00000488954.1:c.107+7392G>C	ENSP00000418504.1:n.107+7392G>C
ENST00000497011.5:c.1112G>C	ENSP00000419505.1:p.Ser371Thr
NM_000055.2:c.1112G>C	NP_000046.1:p.Ser371Thr
XM_005247685.1:c.1235G>C	XP_005247742.1:p.Ser412Thr
NM_000055.3:c.1112G>C	NP_000046.1:p.Ser371Thr
NR_137635.1:n.159+7392G>C
NR_137636.1:n.1279G>C
NM_000055.4:c.1112G>C MANE Select	NP_000046.1:p.Ser371Thr
NR_137635.2:n.110+7392G>C
NR_137636.2:n.1230G>C