Canonical Allele Identifier: CA2229563159

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939989T= , CM000678.2:g.67939989T=	GRCh38
NC_000016.9:g.67973892T= , CM000678.1:g.67973892T=	GRCh37
NC_000016.8:g.66531393T=	NCBI36
NG_009778.1:g.9124A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1238A= MANE Select	ENSP00000264005.5:p.His413=
ENST00000264005.9:c.1238A=	ENSP00000264005.5:p.His413=
ENST00000570369.5:c.241A=
ENST00000573538.5:c.976A=	ENSP00000463220.1:n.976A=
NM_000229.1:c.1238A=	NP_000220.1:p.His413=
NM_000229.2:c.1238A= MANE Select	NP_000220.1:p.His413=