Canonical Allele Identifier: CA2229563332

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940375A= , CM000678.2:g.67940375A=	GRCh38
NC_000016.9:g.67974278A= , CM000678.1:g.67974278A=	GRCh37
NC_000016.8:g.66531779A=	NCBI36
NG_009778.1:g.8738T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.852T= MANE Select	ENSP00000264005.5:p.Pro284=
ENST00000264005.9:c.852T=	ENSP00000264005.5:p.Pro284=
ENST00000570369.5:c.156-301T=
ENST00000570980.1:c.636T=	ENSP00000464651.1:p.Pro212=
ENST00000573538.5:c.590T=	ENSP00000463220.1:n.590T=
NM_000229.1:c.852T=	NP_000220.1:p.Pro284=
NM_000229.2:c.852T= MANE Select	NP_000220.1:p.Pro284=