Canonical Allele Identifier: CA2229563488

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940692C= , CM000678.2:g.67940692C=	GRCh38
NC_000016.9:g.67974595C= , CM000678.1:g.67974595C=	GRCh37
NC_000016.8:g.66532096C=	NCBI36
NG_009778.1:g.8421G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-214G= MANE Select	ENSP00000264005.5:n.749-214G=
ENST00000264005.9:c.749-214G=	ENSP00000264005.5:n.749-214G=
ENST00000570369.5:c.156-618G=
ENST00000570980.1:c.533-214G=	ENSP00000464651.1:n.533-214G=
ENST00000573538.5:c.486+45G=	ENSP00000463220.1:n.486+45G=
NM_000229.1:c.749-214G=	NP_000220.1:n.749-214G=
NM_000229.2:c.749-214G= MANE Select	NP_000220.1:n.749-214G=