Canonical Allele Identifier: CA396375646
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1197469292

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940107T>G , CM000678.2:g.67940107T>G GRCh38
NC_000016.9:g.67974010T>G , CM000678.1:g.67974010T>G GRCh37
NC_000016.8:g.66531511T>G NCBI36
NG_009778.1:g.9006A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1120A>C MANE Select ENSP00000264005.5:p.Thr374Pro
ENST00000264005.9:c.1120A>C ENSP00000264005.5:p.Thr374Pro
ENST00000570369.5:c.156-33A>C
ENST00000573538.5:c.858A>C ENSP00000463220.1:n.858A>C
NM_000229.1:c.1120A>C NP_000220.1:p.Thr374Pro
NM_000229.2:c.1120A>C MANE Select NP_000220.1:p.Thr374Pro