Canonical Allele Identifier: CA2576033577

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942828C>G , CM000678.2:g.67942828C>G	GRCh38
NC_000016.9:g.67976731C>G , CM000678.1:g.67976731C>G	GRCh37
NC_000016.8:g.66534232C>G	NCBI36
NG_009778.1:g.6285G>C
NG_033098.1:g.30867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.427+33G>C MANE Select	ENSP00000264005.5:n.427+33G>C
ENST00000264005.9:c.427+33G>C	ENSP00000264005.5:n.427+33G>C
ENST00000570369.5:c.155+33G>C
ENST00000570980.1:c.211+33G>C	ENSP00000464651.1:n.211+33G>C
ENST00000573538.5:c.70+33G>C	ENSP00000463220.1:n.70+33G>C
ENST00000573846.1:n.41+33G>C
ENST00000575277.1:n.205+33G>C
ENST00000575467.5:c.*122+33G>C	ENSP00000460653.1:n.*122+33G>C
NM_000229.1:c.427+33G>C	NP_000220.1:n.427+33G>C
NM_000229.2:c.427+33G>C MANE Select	NP_000220.1:n.427+33G>C