Canonical Allele Identifier: CA2229563226

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940134A= , CM000678.2:g.67940134A=	GRCh38
NC_000016.9:g.67974037A= , CM000678.1:g.67974037A=	GRCh37
NC_000016.8:g.66531538A=	NCBI36
NG_009778.1:g.8979T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1093T= MANE Select	ENSP00000264005.5:p.Tyr365=
ENST00000264005.9:c.1093T=	ENSP00000264005.5:p.Tyr365=
ENST00000570369.5:c.156-60T=
ENST00000573538.5:c.831T=	ENSP00000463220.1:n.831T=
NM_000229.1:c.1093T=	NP_000220.1:p.Tyr365=
NM_000229.2:c.1093T= MANE Select	NP_000220.1:p.Tyr365=