Canonical Allele Identifier: CA396376168
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940353T>C , CM000678.2:g.67940353T>C GRCh38
NC_000016.9:g.67974256T>C , CM000678.1:g.67974256T>C GRCh37
NC_000016.8:g.66531757T>C NCBI36
NG_009778.1:g.8760A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.874A>G MANE Select ENSP00000264005.5:p.Thr292Ala
ENST00000264005.9:c.874A>G ENSP00000264005.5:p.Thr292Ala
ENST00000570369.5:c.156-279A>G
ENST00000570980.1:c.658A>G ENSP00000464651.1:p.Thr220Ala
ENST00000573538.5:c.612A>G ENSP00000463220.1:n.612A>G
NM_000229.1:c.874A>G NP_000220.1:p.Thr292Ala
NM_000229.2:c.874A>G MANE Select NP_000220.1:p.Thr292Ala