Canonical Allele Identifier: CA396376278
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940402C>A , CM000678.2:g.67940402C>A GRCh38
NC_000016.9:g.67974305C>A , CM000678.1:g.67974305C>A GRCh37
NC_000016.8:g.66531806C>A NCBI36
NG_009778.1:g.8711G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.825G>T MANE Select ENSP00000264005.5:p.Trp275Cys
ENST00000264005.9:c.825G>T ENSP00000264005.5:p.Trp275Cys
ENST00000570369.5:c.156-328G>T
ENST00000570980.1:c.609G>T ENSP00000464651.1:p.Trp203Cys
ENST00000573538.5:c.563G>T ENSP00000463220.1:n.563G>T
NM_000229.1:c.825G>T NP_000220.1:p.Trp275Cys
NM_000229.2:c.825G>T MANE Select NP_000220.1:p.Trp275Cys