Canonical Allele Identifier: CA2229563312

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940331C= , CM000678.2:g.67940331C=	GRCh38
NC_000016.9:g.67974234C= , CM000678.1:g.67974234C=	GRCh37
NC_000016.8:g.66531735C=	NCBI36
NG_009778.1:g.8782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.896G= MANE Select	ENSP00000264005.5:p.Gly299=
ENST00000264005.9:c.896G=	ENSP00000264005.5:p.Gly299=
ENST00000570369.5:c.156-257G=
ENST00000570980.1:c.680G=	ENSP00000464651.1:p.Gly227=
ENST00000573538.5:c.634G=	ENSP00000463220.1:n.634G=
NM_000229.1:c.896G=	NP_000220.1:p.Gly299=
NM_000229.2:c.896G= MANE Select	NP_000220.1:p.Gly299=