Canonical Allele Identifier: CA355112551

Gene: BCHE

Linked Data

• gnomAD v4: 3-165830472-G-T
• MyVariant Identifiers: chr3:g.165548260G>T (hg19) ; chr3:g.165830472G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830472G>T , CM000665.2:g.165830472G>T	GRCh38
NC_000003.11:g.165548260G>T , CM000665.1:g.165548260G>T	GRCh37
NC_000003.10:g.167030954G>T	NCBI36
NG_009031.1:g.11994C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.562C>A MANE Select	ENSP00000264381.3:p.Pro188Thr
ENST00000264381.7:c.562C>A	ENSP00000264381.3:p.Pro188Thr
ENST00000479451.5:c.107+6842C>A	ENSP00000418325.1:n.107+6842C>A
ENST00000482958.1:c.562C>A	ENSP00000419804.1:p.Pro188Thr
ENST00000488954.1:c.107+6842C>A	ENSP00000418504.1:n.107+6842C>A
ENST00000497011.5:c.562C>A	ENSP00000419505.1:p.Pro188Thr
NM_000055.2:c.562C>A	NP_000046.1:p.Pro188Thr
XM_005247685.1:c.685C>A	XP_005247742.1:p.Pro229Thr
NM_000055.3:c.562C>A	NP_000046.1:p.Pro188Thr
NR_137635.1:n.159+6842C>A
NR_137636.1:n.729C>A
NM_000055.4:c.562C>A MANE Select	NP_000046.1:p.Pro188Thr
NR_137635.2:n.110+6842C>A
NR_137636.2:n.680C>A