Canonical Allele Identifier: CA396375630
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940099G>T , CM000678.2:g.67940099G>T GRCh38
NC_000016.9:g.67974002G>T , CM000678.1:g.67974002G>T GRCh37
NC_000016.8:g.66531503G>T NCBI36
NG_009778.1:g.9014C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1128C>A MANE Select ENSP00000264005.5:p.Ser376Arg
ENST00000264005.9:c.1128C>A ENSP00000264005.5:p.Ser376Arg
ENST00000570369.5:c.156-25C>A
ENST00000573538.5:c.866C>A ENSP00000463220.1:n.866C>A
NM_000229.1:c.1128C>A NP_000220.1:p.Ser376Arg
NM_000229.2:c.1128C>A MANE Select NP_000220.1:p.Ser376Arg