Canonical Allele Identifier: CA2229563149

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939962T= , CM000678.2:g.67939962T=	GRCh38
NC_000016.9:g.67973865T= , CM000678.1:g.67973865T=	GRCh37
NC_000016.8:g.66531366T=	NCBI36
NG_009778.1:g.9151A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1265A= MANE Select	ENSP00000264005.5:p.Tyr422=
ENST00000264005.9:c.1265A=	ENSP00000264005.5:p.Tyr422=
ENST00000570369.5:c.268A=
ENST00000573538.5:c.1003A=	ENSP00000463220.1:n.1003A=
NM_000229.1:c.1265A=	NP_000220.1:p.Tyr422=
NM_000229.2:c.1265A= MANE Select	NP_000220.1:p.Tyr422=