Canonical Allele Identifier: CA2229563210
Gene: LCAT HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1120A= MANE Select ENSP00000264005.5:p.Thr374=
ENST00000264005.9:c.1120A= ENSP00000264005.5:p.Thr374=
ENST00000570369.5:c.156-33A=
ENST00000573538.5:c.858A= ENSP00000463220.1:n.858A=
NM_000229.1:c.1120A= NP_000220.1:p.Thr374=
NM_000229.2:c.1120A= MANE Select NP_000220.1:p.Thr374=