Canonical Allele Identifier: CA2633852021
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940829T>A , CM000678.2:g.67940829T>A GRCh38
NC_000016.9:g.67974732T>A , CM000678.1:g.67974732T>A GRCh37
NC_000016.8:g.66532233T>A NCBI36
NG_009778.1:g.8284A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-351A>T MANE Select ENSP00000264005.5:n.749-351A>T
ENST00000264005.9:c.749-351A>T ENSP00000264005.5:n.749-351A>T
ENST00000570369.5:c.156-755A>T
ENST00000570980.1:c.533-351A>T ENSP00000464651.1:n.533-351A>T
ENST00000573538.5:c.394A>T ENSP00000463220.1:p.Thr132Ser
NM_000229.1:c.749-351A>T NP_000220.1:n.749-351A>T
NM_000229.2:c.749-351A>T MANE Select NP_000220.1:n.749-351A>T