Canonical Allele Identifier: CA2229563183
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940053G= , CM000678.2:g.67940053G= GRCh38
NC_000016.9:g.67973956G= , CM000678.1:g.67973956G= GRCh37
NC_000016.8:g.66531457G= NCBI36
NG_009778.1:g.9060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1174C= MANE Select ENSP00000264005.5:p.His392=
ENST00000264005.9:c.1174C= ENSP00000264005.5:p.His392=
ENST00000570369.5:c.177C=
ENST00000573538.5:c.912C= ENSP00000463220.1:n.912C=
NM_000229.1:c.1174C= NP_000220.1:p.His392=
NM_000229.2:c.1174C= MANE Select NP_000220.1:p.His392=