Canonical Allele Identifier: CA2229563179
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940045C= , CM000678.2:g.67940045C= GRCh38
NC_000016.9:g.67973948C= , CM000678.1:g.67973948C= GRCh37
NC_000016.8:g.66531449C= NCBI36
NG_009778.1:g.9068G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1182G= MANE Select ENSP00000264005.5:p.Leu394=
ENST00000264005.9:c.1182G= ENSP00000264005.5:p.Leu394=
ENST00000570369.5:c.185G=
ENST00000573538.5:c.920G= ENSP00000463220.1:n.920G=
NM_000229.1:c.1182G= NP_000220.1:p.Leu394=
NM_000229.2:c.1182G= MANE Select NP_000220.1:p.Leu394=