Canonical Allele Identifier: CA2229563523
Gene: LCAT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940761G= , CM000678.2:g.67940761G= GRCh38
NC_000016.9:g.67974664G= , CM000678.1:g.67974664G= GRCh37
NC_000016.8:g.66532165G= NCBI36
NG_009778.1:g.8352C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-283C= MANE Select ENSP00000264005.5:n.749-283C=
ENST00000264005.9:c.749-283C= ENSP00000264005.5:n.749-283C=
ENST00000570369.5:c.156-687C=
ENST00000570980.1:c.533-283C= ENSP00000464651.1:n.533-283C=
ENST00000573538.5:c.462C= ENSP00000463220.1:n.462C=
NM_000229.1:c.749-283C= NP_000220.1:n.749-283C=
NM_000229.2:c.749-283C= MANE Select NP_000220.1:n.749-283C=
Search 100 bp 5'
Search 100 bp 3'