Canonical Allele Identifier: CA2633851961
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940816C>T , CM000678.2:g.67940816C>T GRCh38
NC_000016.9:g.67974719C>T , CM000678.1:g.67974719C>T GRCh37
NC_000016.8:g.66532220C>T NCBI36
NG_009778.1:g.8297G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-338G>A MANE Select ENSP00000264005.5:n.749-338G>A
ENST00000264005.9:c.749-338G>A ENSP00000264005.5:n.749-338G>A
ENST00000570369.5:c.156-742G>A
ENST00000570980.1:c.533-338G>A ENSP00000464651.1:n.533-338G>A
ENST00000573538.5:c.407G>A ENSP00000463220.1:p.Cys136Tyr
NM_000229.1:c.749-338G>A NP_000220.1:n.749-338G>A
NM_000229.2:c.749-338G>A MANE Select NP_000220.1:n.749-338G>A