Canonical Allele Identifier: CA2565338800

Gene: BCHE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165786493T>A , CM000665.2:g.165786493T>A	GRCh38
NC_000003.11:g.165504281T>A , CM000665.1:g.165504281T>A	GRCh37
NC_000003.10:g.166986975T>A	NCBI36
NG_009031.1:g.55973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264381.8:c.1518-182A>T MANE Select	ENSP00000264381.3:n.1518-182A>T
ENST00000264381.7:c.1518-182A>T	ENSP00000264381.3:n.1518-182A>T
ENST00000479451.5:c.108-182A>T	ENSP00000418325.1:n.108-182A>T
ENST00000482958.1:c.*24-182A>T	ENSP00000419804.1:n.*24-182A>T
ENST00000488954.1:c.108-182A>T	ENSP00000418504.1:n.108-182A>T
ENST00000497011.5:c.1518-182A>T	ENSP00000419505.1:n.1518-182A>T
NM_000055.2:c.1518-182A>T	NP_000046.1:n.1518-182A>T
XM_005247685.1:c.1641-182A>T	XP_005247742.1:n.1641-182A>T
NM_000055.3:c.1518-182A>T	NP_000046.1:n.1518-182A>T
NR_137635.1:n.160-182A>T
NR_137636.1:n.1685-182A>T
NM_000055.4:c.1518-182A>T MANE Select	NP_000046.1:n.1518-182A>T
NR_137635.2:n.111-182A>T
NR_137636.2:n.1636-182A>T