Canonical Allele Identifier: CA396376356
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940439A>G , CM000678.2:g.67940439A>G GRCh38
NC_000016.9:g.67974342A>G , CM000678.1:g.67974342A>G GRCh37
NC_000016.8:g.66531843A>G NCBI36
NG_009778.1:g.8674T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.788T>C MANE Select ENSP00000264005.5:p.Leu263Pro
ENST00000264005.9:c.788T>C ENSP00000264005.5:p.Leu263Pro
ENST00000570369.5:c.156-365T>C
ENST00000570980.1:c.572T>C ENSP00000464651.1:p.Leu191Pro
ENST00000573538.5:c.526T>C ENSP00000463220.1:n.526T>C
NM_000229.1:c.788T>C NP_000220.1:p.Leu263Pro
NM_000229.2:c.788T>C MANE Select NP_000220.1:p.Leu263Pro