Canonical Allele Identifier: CA396376231
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940380A>T , CM000678.2:g.67940380A>T GRCh38
NC_000016.9:g.67974283A>T , CM000678.1:g.67974283A>T GRCh37
NC_000016.8:g.66531784A>T NCBI36
NG_009778.1:g.8733T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.847T>A MANE Select ENSP00000264005.5:p.Trp283Arg
ENST00000264005.9:c.847T>A ENSP00000264005.5:p.Trp283Arg
ENST00000570369.5:c.156-306T>A
ENST00000570980.1:c.631T>A ENSP00000464651.1:p.Trp211Arg
ENST00000573538.5:c.585T>A ENSP00000463220.1:n.585T>A
NM_000229.1:c.847T>A NP_000220.1:p.Trp283Arg
NM_000229.2:c.847T>A MANE Select NP_000220.1:p.Trp283Arg