Canonical Allele Identifier: CA2229564619
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67942945A= , CM000678.2:g.67942945A= GRCh38
NC_000016.9:g.67976848A= , CM000678.1:g.67976848A= GRCh37
NC_000016.8:g.66534349A= NCBI36
NG_009778.1:g.6168T=
NG_033098.1:g.30750T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.343T= MANE Select ENSP00000264005.5:p.Ser115=
ENST00000264005.9:c.343T= ENSP00000264005.5:p.Ser115=
ENST00000570369.5:c.71T=
ENST00000570980.1:c.127T= ENSP00000464651.1:p.Ser43=
ENST00000575277.1:n.121T=
ENST00000575467.5:c.*38T= ENSP00000460653.1:n.*38T=
NM_000229.1:c.343T= NP_000220.1:p.Ser115=
NM_000229.2:c.343T= MANE Select NP_000220.1:p.Ser115=