Canonical Allele Identifier: CA355110659

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829604G>C , CM000665.2:g.165829604G>C	GRCh38
NC_000003.11:g.165547392G>C , CM000665.1:g.165547392G>C	GRCh37
NC_000003.10:g.167030086G>C	NCBI36
NG_009031.1:g.12862C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000055.4:c.1430C>G MANE Select	NP_000046.1:p.Pro477Arg
ENST00000264381.8:c.1430C>G MANE Select	ENSP00000264381.3:p.Pro477Arg
NM_000055.2:c.1430C>G	NP_000046.1:p.Pro477Arg
NM_000055.3:c.1430C>G	NP_000046.1:p.Pro477Arg
NR_137635.1:n.159+7710C>G
NR_137635.2:n.110+7710C>G
NR_137636.1:n.1597C>G
NR_137636.2:n.1548C>G
ENST00000264381.7:c.1430C>G	ENSP00000264381.3:p.Pro477Arg
ENST00000479451.5:c.107+7710C>G	ENSP00000418325.1:n.107+7710C>G
ENST00000482958.1:c.1430C>G	ENSP00000419804.1:p.Pro477Arg
ENST00000488954.1:c.107+7710C>G	ENSP00000418504.1:n.107+7710C>G
ENST00000497011.5:c.1430C>G	ENSP00000419505.1:p.Pro477Arg
XM_005247685.1:c.1553C>G	XP_005247742.1:p.Pro518Arg