Canonical Allele Identifier: CA2229564568

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942827G= , CM000678.2:g.67942827G=	GRCh38
NC_000016.9:g.67976730G= , CM000678.1:g.67976730G=	GRCh37
NC_000016.8:g.66534231G=	NCBI36
NG_009778.1:g.6286C=
NG_033098.1:g.30868C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.427+34C= MANE Select	ENSP00000264005.5:n.427+34C=
ENST00000264005.9:c.427+34C=	ENSP00000264005.5:n.427+34C=
ENST00000570369.5:c.155+34C=
ENST00000570980.1:c.211+34C=	ENSP00000464651.1:n.211+34C=
ENST00000573538.5:c.70+34C=	ENSP00000463220.1:n.70+34C=
ENST00000573846.1:n.41+34C=
ENST00000575277.1:n.205+34C=
ENST00000575467.5:c.*122+34C=	ENSP00000460653.1:n.*122+34C=
NM_000229.1:c.427+34C=	NP_000220.1:n.427+34C=
NM_000229.2:c.427+34C= MANE Select	NP_000220.1:n.427+34C=