Canonical Allele Identifier: CA2229563537
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs908342252

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940807T>G , CM000678.2:g.67940807T>G GRCh38
NC_000016.9:g.67974710T>G , CM000678.1:g.67974710T>G GRCh37
NC_000016.8:g.66532211T>G NCBI36
NG_009778.1:g.8306A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-329A>C MANE Select ENSP00000264005.5:n.749-329A>C
ENST00000264005.9:c.749-329A>C ENSP00000264005.5:n.749-329A>C
ENST00000570369.5:c.156-733A>C
ENST00000570980.1:c.533-329A>C ENSP00000464651.1:n.533-329A>C
ENST00000573538.5:c.416A>C ENSP00000463220.1:p.Ter139Ser
NM_000229.1:c.749-329A>C NP_000220.1:n.749-329A>C
NM_000229.2:c.749-329A>C MANE Select NP_000220.1:n.749-329A>C