Canonical Allele Identifier: CA2807445497
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940783del , CM000678.2:g.67940783del GRCh38
NC_000016.9:g.67974686del , CM000678.1:g.67974686del GRCh37
NC_000016.8:g.66532187del NCBI36
NG_009778.1:g.8330del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-305del MANE Select ENSP00000264005.5:n.749-305del
ENST00000264005.9:c.749-305del ENSP00000264005.5:n.749-305del
ENST00000570369.5:c.156-709del
ENST00000570980.1:c.533-305del ENSP00000464651.1:n.533-305del
ENST00000573538.5:c.440del ENSP00000463220.1:n.440del
NM_000229.1:c.749-305del NP_000220.1:n.749-305del
NM_000229.2:c.749-305del MANE Select NP_000220.1:n.749-305del