Canonical Allele Identifier: CA2229563321

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940355G= , CM000678.2:g.67940355G=	GRCh38
NC_000016.9:g.67974258G= , CM000678.1:g.67974258G=	GRCh37
NC_000016.8:g.66531759G=	NCBI36
NG_009778.1:g.8758C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.872C= MANE Select	ENSP00000264005.5:p.Ser291=
ENST00000264005.9:c.872C=	ENSP00000264005.5:p.Ser291=
ENST00000570369.5:c.156-281C=
ENST00000570980.1:c.656C=	ENSP00000464651.1:p.Ser219=
ENST00000573538.5:c.610C=	ENSP00000463220.1:n.610C=
NM_000229.1:c.872C=	NP_000220.1:p.Ser291=
NM_000229.2:c.872C= MANE Select	NP_000220.1:p.Ser291=