Canonical Allele Identifier: CA396376276
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940401T>C , CM000678.2:g.67940401T>C GRCh38
NC_000016.9:g.67974304T>C , CM000678.1:g.67974304T>C GRCh37
NC_000016.8:g.66531805T>C NCBI36
NG_009778.1:g.8712A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.826A>G MANE Select ENSP00000264005.5:p.Met276Val
ENST00000264005.9:c.826A>G ENSP00000264005.5:p.Met276Val
ENST00000570369.5:c.156-327A>G
ENST00000570980.1:c.610A>G ENSP00000464651.1:p.Met204Val
ENST00000573538.5:c.564A>G ENSP00000463220.1:n.564A>G
NM_000229.1:c.826A>G NP_000220.1:p.Met276Val
NM_000229.2:c.826A>G MANE Select NP_000220.1:p.Met276Val