Canonical Allele Identifier: CA355113786

Gene: BCHE

Linked Data

• MyVariant Identifiers: chr3:g.165491183C>G (hg19) ; chr3:g.165773395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165773395C>G , CM000665.2:g.165773395C>G	GRCh38
NC_000003.11:g.165491183C>G , CM000665.1:g.165491183C>G	GRCh37
NC_000003.10:g.166973877C>G	NCBI36
NG_009031.1:g.69071G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264381.8:c.1796G>C MANE Select	ENSP00000264381.3:p.Cys599Ser
ENST00000264381.7:c.1796G>C	ENSP00000264381.3:p.Cys599Ser
ENST00000479451.5:c.386G>C	ENSP00000418325.1:p.Cys129Ser
ENST00000482958.1:c.*302G>C	ENSP00000419804.1:n.*302G>C
ENST00000497011.5:c.*186G>C	ENSP00000419505.1:n.*186G>C
NM_000055.2:c.1796G>C	NP_000046.1:p.Cys599Ser
XM_005247685.1:c.1919G>C	XP_005247742.1:p.Cys640Ser
NM_000055.3:c.1796G>C	NP_000046.1:p.Cys599Ser
NR_137635.1:n.438G>C
NR_137636.1:n.2042G>C
NM_000055.4:c.1796G>C MANE Select	NP_000046.1:p.Cys599Ser
NR_137635.2:n.389G>C
NR_137636.2:n.1993G>C