Canonical Allele Identifier: CA2229563156

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939982A= , CM000678.2:g.67939982A=	GRCh38
NC_000016.9:g.67973885A= , CM000678.1:g.67973885A=	GRCh37
NC_000016.8:g.66531386A=	NCBI36
NG_009778.1:g.9131T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1245T= MANE Select	ENSP00000264005.5:p.Asn415=
ENST00000264005.9:c.1245T=	ENSP00000264005.5:p.Asn415=
ENST00000570369.5:c.248T=
ENST00000573538.5:c.983T=	ENSP00000463220.1:n.983T=
NM_000229.1:c.1245T=	NP_000220.1:p.Asn415=
NM_000229.2:c.1245T= MANE Select	NP_000220.1:p.Asn415=