Canonical Allele Identifier: CA2229563389

Gene: LCAT

Linked Data

• dbSNP Id: rs2058286314

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940514G>A , CM000678.2:g.67940514G>A	GRCh38
NC_000016.9:g.67974417G>A , CM000678.1:g.67974417G>A	GRCh37
NC_000016.8:g.66531918G>A	NCBI36
NG_009778.1:g.8599C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.749-36C>T MANE Select	ENSP00000264005.5:n.749-36C>T
ENST00000264005.9:c.749-36C>T	ENSP00000264005.5:n.749-36C>T
ENST00000570369.5:c.156-440C>T
ENST00000570980.1:c.533-36C>T	ENSP00000464651.1:n.533-36C>T
ENST00000573538.5:c.487-36C>T	ENSP00000463220.1:n.487-36C>T
NM_000229.1:c.749-36C>T	NP_000220.1:n.749-36C>T
NM_000229.2:c.749-36C>T MANE Select	NP_000220.1:n.749-36C>T