Canonical Allele Identifier: CA355111022

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165829764A>G , CM000665.2:g.165829764A>G	GRCh38
NC_000003.11:g.165547552A>G , CM000665.1:g.165547552A>G	GRCh37
NC_000003.10:g.167030246A>G	NCBI36
NG_009031.1:g.12702T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000055.4:c.1270T>C MANE Select	NP_000046.1:p.Tyr424His
ENST00000264381.8:c.1270T>C MANE Select	ENSP00000264381.3:p.Tyr424His
NM_000055.2:c.1270T>C	NP_000046.1:p.Tyr424His
NM_000055.3:c.1270T>C	NP_000046.1:p.Tyr424His
NR_137635.1:n.159+7550T>C
NR_137635.2:n.110+7550T>C
NR_137636.1:n.1437T>C
NR_137636.2:n.1388T>C
ENST00000264381.7:c.1270T>C	ENSP00000264381.3:p.Tyr424His
ENST00000479451.5:c.107+7550T>C	ENSP00000418325.1:n.107+7550T>C
ENST00000482958.1:c.1270T>C	ENSP00000419804.1:p.Tyr424His
ENST00000488954.1:c.107+7550T>C	ENSP00000418504.1:n.107+7550T>C
ENST00000497011.5:c.1270T>C	ENSP00000419505.1:p.Tyr424His
XM_005247685.1:c.1393T>C	XP_005247742.1:p.Tyr465His