Canonical Allele Identifier: CA2229563381
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940506G= , CM000678.2:g.67940506G= GRCh38
NC_000016.9:g.67974409G= , CM000678.1:g.67974409G= GRCh37
NC_000016.8:g.66531910G= NCBI36
NG_009778.1:g.8607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-28C= MANE Select ENSP00000264005.5:n.749-28C=
ENST00000264005.9:c.749-28C= ENSP00000264005.5:n.749-28C=
ENST00000570369.5:c.156-432C=
ENST00000570980.1:c.533-28C= ENSP00000464651.1:n.533-28C=
ENST00000573538.5:c.487-28C= ENSP00000463220.1:n.487-28C=
NM_000229.1:c.749-28C= NP_000220.1:n.749-28C=
NM_000229.2:c.749-28C= MANE Select NP_000220.1:n.749-28C=