Canonical Allele Identifier: CA2229563313

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940334G= , CM000678.2:g.67940334G=	GRCh38
NC_000016.9:g.67974237G= , CM000678.1:g.67974237G=	GRCh37
NC_000016.8:g.66531738G=	NCBI36
NG_009778.1:g.8779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.893C= MANE Select	ENSP00000264005.5:p.Thr298=
ENST00000264005.9:c.893C=	ENSP00000264005.5:p.Thr298=
ENST00000570369.5:c.156-260C=
ENST00000570980.1:c.677C=	ENSP00000464651.1:p.Thr226=
ENST00000573538.5:c.631C=	ENSP00000463220.1:n.631C=
NM_000229.1:c.893C=	NP_000220.1:p.Thr298=
NM_000229.2:c.893C= MANE Select	NP_000220.1:p.Thr298=