Canonical Allele Identifier: CA2229563192
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940070C= , CM000678.2:g.67940070C= GRCh38
NC_000016.9:g.67973973C= , CM000678.1:g.67973973C= GRCh37
NC_000016.8:g.66531474C= NCBI36
NG_009778.1:g.9043G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1157G= MANE Select ENSP00000264005.5:p.Arg386=
ENST00000264005.9:c.1157G= ENSP00000264005.5:p.Arg386=
ENST00000570369.5:c.160G=
ENST00000573538.5:c.895G= ENSP00000463220.1:n.895G=
NM_000229.1:c.1157G= NP_000220.1:p.Arg386=
NM_000229.2:c.1157G= MANE Select NP_000220.1:p.Arg386=