Canonical Allele Identifier: CA2229563339

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940393G= , CM000678.2:g.67940393G=	GRCh38
NC_000016.9:g.67974296G= , CM000678.1:g.67974296G=	GRCh37
NC_000016.8:g.66531797G=	NCBI36
NG_009778.1:g.8720C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.834C= MANE Select	ENSP00000264005.5:p.Pro278=
ENST00000264005.9:c.834C=	ENSP00000264005.5:p.Pro278=
ENST00000570369.5:c.156-319C=
ENST00000570980.1:c.618C=	ENSP00000464651.1:p.Pro206=
ENST00000573538.5:c.572C=	ENSP00000463220.1:n.572C=
NM_000229.1:c.834C=	NP_000220.1:p.Pro278=
NM_000229.2:c.834C= MANE Select	NP_000220.1:p.Pro278=