Canonical Allele Identifier: CA396376044
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940298T>C , CM000678.2:g.67940298T>C GRCh38
NC_000016.9:g.67974201T>C , CM000678.1:g.67974201T>C GRCh37
NC_000016.8:g.66531702T>C NCBI36
NG_009778.1:g.8815A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.929A>G MANE Select ENSP00000264005.5:p.His310Arg
ENST00000264005.9:c.929A>G ENSP00000264005.5:p.His310Arg
ENST00000570369.5:c.156-224A>G
ENST00000570980.1:c.713A>G ENSP00000464651.1:p.His238Arg
ENST00000573538.5:c.667A>G ENSP00000463220.1:n.667A>G
NM_000229.1:c.929A>G NP_000220.1:p.His310Arg
NM_000229.2:c.929A>G MANE Select NP_000220.1:p.His310Arg