Canonical Allele Identifier: CA2229563157

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939983T= , CM000678.2:g.67939983T=	GRCh38
NC_000016.9:g.67973886T= , CM000678.1:g.67973886T=	GRCh37
NC_000016.8:g.66531387T=	NCBI36
NG_009778.1:g.9130A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1244A= MANE Select	ENSP00000264005.5:p.Asn415=
ENST00000264005.9:c.1244A=	ENSP00000264005.5:p.Asn415=
ENST00000570369.5:c.247A=
ENST00000573538.5:c.982A=	ENSP00000463220.1:n.982A=
NM_000229.1:c.1244A=	NP_000220.1:p.Asn415=
NM_000229.2:c.1244A= MANE Select	NP_000220.1:p.Asn415=