Canonical Allele Identifier: CA355111363

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165547705T>A (hg19) ; chr3:g.165829917T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829917T>A , CM000665.2:g.165829917T>A	GRCh38
NC_000003.11:g.165547705T>A , CM000665.1:g.165547705T>A	GRCh37
NC_000003.10:g.167030399T>A	NCBI36
NG_009031.1:g.12549A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1117A>T MANE Select	ENSP00000264381.3:p.Ile373Leu
ENST00000264381.7:c.1117A>T	ENSP00000264381.3:p.Ile373Leu
ENST00000479451.5:c.107+7397A>T	ENSP00000418325.1:n.107+7397A>T
ENST00000482958.1:c.1117A>T	ENSP00000419804.1:p.Ile373Leu
ENST00000488954.1:c.107+7397A>T	ENSP00000418504.1:n.107+7397A>T
ENST00000497011.5:c.1117A>T	ENSP00000419505.1:p.Ile373Leu
NM_000055.2:c.1117A>T	NP_000046.1:p.Ile373Leu
XM_005247685.1:c.1240A>T	XP_005247742.1:p.Ile414Leu
NM_000055.3:c.1117A>T	NP_000046.1:p.Ile373Leu
NR_137635.1:n.159+7397A>T
NR_137636.1:n.1284A>T
NM_000055.4:c.1117A>T MANE Select	NP_000046.1:p.Ile373Leu
NR_137635.2:n.110+7397A>T
NR_137636.2:n.1235A>T