Canonical Allele Identifier: CA2229563150

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939967A= , CM000678.2:g.67939967A=	GRCh38
NC_000016.9:g.67973870A= , CM000678.1:g.67973870A=	GRCh37
NC_000016.8:g.66531371A=	NCBI36
NG_009778.1:g.9146T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1260T= MANE Select	ENSP00000264005.5:p.Gly420=
ENST00000264005.9:c.1260T=	ENSP00000264005.5:p.Gly420=
ENST00000570369.5:c.263T=
ENST00000573538.5:c.998T=	ENSP00000463220.1:n.998T=
NM_000229.1:c.1260T=	NP_000220.1:p.Gly420=
NM_000229.2:c.1260T= MANE Select	NP_000220.1:p.Gly420=