Canonical Allele Identifier: CA2633852109
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940835_67940837del , CM000678.2:g.67940835_67940837del GRCh38
NC_000016.9:g.67974738_67974740del , CM000678.1:g.67974738_67974740del GRCh37
NC_000016.8:g.66532239_66532241del NCBI36
NG_009778.1:g.8277_8279del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-358_749-356del MANE Select ENSP00000264005.5:n.749-358_749-356del
ENST00000264005.9:c.749-358_749-356del ENSP00000264005.5:n.749-358_749-356del
ENST00000570369.5:c.156-762_156-760del
ENST00000570980.1:c.533-358_533-356del ENSP00000464651.1:n.533-358_533-356del
ENST00000573538.5:c.392-5_392-3del ENSP00000463220.1:n.392-5_392-3del
NM_000229.1:c.749-358_749-356del NP_000220.1:n.749-358_749-356del
NM_000229.2:c.749-358_749-356del MANE Select NP_000220.1:n.749-358_749-356del