Canonical Allele Identifier: CA2229563212
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940109G= , CM000678.2:g.67940109G= GRCh38
NC_000016.9:g.67974012G= , CM000678.1:g.67974012G= GRCh37
NC_000016.8:g.66531513G= NCBI36
NG_009778.1:g.9004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1118C= MANE Select ENSP00000264005.5:p.Ala373=
ENST00000264005.9:c.1118C= ENSP00000264005.5:p.Ala373=
ENST00000570369.5:c.156-35C=
ENST00000573538.5:c.856C= ENSP00000463220.1:n.856C=
NM_000229.1:c.1118C= NP_000220.1:p.Ala373=
NM_000229.2:c.1118C= MANE Select NP_000220.1:p.Ala373=