Canonical Allele Identifier: CA436969355

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165548687G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165830899G>A , CM000665.2:g.165830899G>A	GRCh38
NC_000003.11:g.165548687G>A , CM000665.1:g.165548687G>A	GRCh37
NC_000003.10:g.167031381G>A	NCBI36
NG_009031.1:g.11567C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.135C>T MANE Select	ENSP00000264381.3:p.Asn45=
ENST00000264381.7:c.135C>T	ENSP00000264381.3:p.Asn45=
ENST00000479451.5:c.107+6415C>T	ENSP00000418325.1:n.107+6415C>T
ENST00000482958.1:c.135C>T	ENSP00000419804.1:p.Asn45=
ENST00000488954.1:c.107+6415C>T	ENSP00000418504.1:n.107+6415C>T
ENST00000497011.5:c.135C>T	ENSP00000419505.1:p.Asn45=
NM_000055.2:c.135C>T	NP_000046.1:p.Asn45=
XM_005247685.1:c.258C>T	XP_005247742.1:p.Asn86=
NM_000055.3:c.135C>T	NP_000046.1:p.Asn45=
NR_137635.1:n.159+6415C>T
NR_137636.1:n.302C>T
NM_000055.4:c.135C>T MANE Select	NP_000046.1:p.Asn45=
NR_137635.2:n.110+6415C>T
NR_137636.2:n.253C>T