Canonical Allele Identifier: CA87410369

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830652G>A , CM000665.2:g.165830652G>A	GRCh38
NC_000003.11:g.165548440G>A , CM000665.1:g.165548440G>A	GRCh37
NC_000003.10:g.167031134G>A	NCBI36
NG_009031.1:g.11814C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000055.4:c.382C>T MANE Select	NP_000046.1:p.Pro128Ser
ENST00000264381.8:c.382C>T MANE Select	ENSP00000264381.3:p.Pro128Ser
NM_000055.2:c.382C>T	NP_000046.1:p.Pro128Ser
NM_000055.3:c.382C>T	NP_000046.1:p.Pro128Ser
NR_137635.1:n.159+6662C>T
NR_137635.2:n.110+6662C>T
NR_137636.1:n.549C>T
NR_137636.2:n.500C>T
ENST00000264381.7:c.382C>T	ENSP00000264381.3:p.Pro128Ser
ENST00000479451.5:c.107+6662C>T	ENSP00000418325.1:n.107+6662C>T
ENST00000482958.1:c.382C>T	ENSP00000419804.1:p.Pro128Ser
ENST00000488954.1:c.107+6662C>T	ENSP00000418504.1:n.107+6662C>T
ENST00000497011.5:c.382C>T	ENSP00000419505.1:p.Pro128Ser
XM_005247685.1:c.505C>T	XP_005247742.1:p.Pro169Ser