Canonical Allele Identifier: CA2633851928
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940813A>C , CM000678.2:g.67940813A>C GRCh38
NC_000016.9:g.67974716A>C , CM000678.1:g.67974716A>C GRCh37
NC_000016.8:g.66532217A>C NCBI36
NG_009778.1:g.8300T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-335T>G MANE Select ENSP00000264005.5:n.749-335T>G
ENST00000264005.9:c.749-335T>G ENSP00000264005.5:n.749-335T>G
ENST00000570369.5:c.156-739T>G
ENST00000570980.1:c.533-335T>G ENSP00000464651.1:n.533-335T>G
ENST00000573538.5:c.410T>G ENSP00000463220.1:p.Ile137Ser
NM_000229.1:c.749-335T>G NP_000220.1:n.749-335T>G
NM_000229.2:c.749-335T>G MANE Select NP_000220.1:n.749-335T>G