Canonical Allele Identifier: CA2229563314

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940336G= , CM000678.2:g.67940336G=	GRCh38
NC_000016.9:g.67974239G= , CM000678.1:g.67974239G=	GRCh37
NC_000016.8:g.66531740G=	NCBI36
NG_009778.1:g.8777C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.891C= MANE Select	ENSP00000264005.5:p.Tyr297=
ENST00000264005.9:c.891C=	ENSP00000264005.5:p.Tyr297=
ENST00000570369.5:c.156-262C=
ENST00000570980.1:c.675C=	ENSP00000464651.1:p.Tyr225=
ENST00000573538.5:c.629C=	ENSP00000463220.1:n.629C=
NM_000229.1:c.891C=	NP_000220.1:p.Tyr297=
NM_000229.2:c.891C= MANE Select	NP_000220.1:p.Tyr297=