Canonical Allele Identifier: CA2229564650

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67943002A= , CM000678.2:g.67943002A=	GRCh38
NC_000016.9:g.67976905A= , CM000678.1:g.67976905A=	GRCh37
NC_000016.8:g.66534406A=	NCBI36
NG_009778.1:g.6111T=
NG_033098.1:g.30693T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.312-26T= MANE Select	ENSP00000264005.5:n.312-26T=
ENST00000264005.9:c.312-26T=	ENSP00000264005.5:n.312-26T=
ENST00000570369.5:c.40-26T=
ENST00000570980.1:c.96-26T=	ENSP00000464651.1:n.96-26T=
ENST00000575277.1:n.90-26T=
ENST00000575467.5:c.*7-26T=	ENSP00000460653.1:n.*7-26T=
NM_000229.1:c.312-26T=	NP_000220.1:n.312-26T=
NM_000229.2:c.312-26T= MANE Select	NP_000220.1:n.312-26T=