Canonical Allele Identifier: CA2229564655

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67943012C= , CM000678.2:g.67943012C=	GRCh38
NC_000016.9:g.67976915C= , CM000678.1:g.67976915C=	GRCh37
NC_000016.8:g.66534416C=	NCBI36
NG_009778.1:g.6101G=
NG_033098.1:g.30683G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.312-36G= MANE Select	ENSP00000264005.5:n.312-36G=
ENST00000264005.9:c.312-36G=	ENSP00000264005.5:n.312-36G=
ENST00000570369.5:c.40-36G=
ENST00000570980.1:c.96-36G=	ENSP00000464651.1:n.96-36G=
ENST00000575277.1:n.90-36G=
ENST00000575467.5:c.*7-36G=	ENSP00000460653.1:n.*7-36G=
NM_000229.1:c.312-36G=	NP_000220.1:n.312-36G=
NM_000229.2:c.312-36G= MANE Select	NP_000220.1:n.312-36G=