Canonical Allele Identifier: CA396375695
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940130T>G , CM000678.2:g.67940130T>G GRCh38
NC_000016.9:g.67974033T>G , CM000678.1:g.67974033T>G GRCh37
NC_000016.8:g.66531534T>G NCBI36
NG_009778.1:g.8983A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1097A>C MANE Select ENSP00000264005.5:p.Glu366Ala
ENST00000264005.9:c.1097A>C ENSP00000264005.5:p.Glu366Ala
ENST00000570369.5:c.156-56A>C
ENST00000573538.5:c.835A>C ENSP00000463220.1:n.835A>C
NM_000229.1:c.1097A>C NP_000220.1:p.Glu366Ala
NM_000229.2:c.1097A>C MANE Select NP_000220.1:p.Glu366Ala