Canonical Allele Identifier: CA2229563529

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940775G= , CM000678.2:g.67940775G=	GRCh38
NC_000016.9:g.67974678G= , CM000678.1:g.67974678G=	GRCh37
NC_000016.8:g.66532179G=	NCBI36
NG_009778.1:g.8338C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-297C= MANE Select	ENSP00000264005.5:n.749-297C=
ENST00000264005.9:c.749-297C=	ENSP00000264005.5:n.749-297C=
ENST00000570369.5:c.156-701C=
ENST00000570980.1:c.533-297C=	ENSP00000464651.1:n.533-297C=
ENST00000573538.5:c.448C=	ENSP00000463220.1:n.448C=
NM_000229.1:c.749-297C=	NP_000220.1:n.749-297C=
NM_000229.2:c.749-297C= MANE Select	NP_000220.1:n.749-297C=