Canonical Allele Identifier: CA2576033579

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942840G>C , CM000678.2:g.67942840G>C	GRCh38
NC_000016.9:g.67976743G>C , CM000678.1:g.67976743G>C	GRCh37
NC_000016.8:g.66534244G>C	NCBI36
NG_009778.1:g.6273C>G
NG_033098.1:g.30855C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.427+21C>G MANE Select	ENSP00000264005.5:n.427+21C>G
ENST00000264005.9:c.427+21C>G	ENSP00000264005.5:n.427+21C>G
ENST00000570369.5:c.155+21C>G
ENST00000570980.1:c.211+21C>G	ENSP00000464651.1:n.211+21C>G
ENST00000573538.5:c.70+21C>G	ENSP00000463220.1:n.70+21C>G
ENST00000573846.1:n.41+21C>G
ENST00000575277.1:n.205+21C>G
ENST00000575467.5:c.*122+21C>G	ENSP00000460653.1:n.*122+21C>G
NM_000229.1:c.427+21C>G	NP_000220.1:n.427+21C>G
NM_000229.2:c.427+21C>G MANE Select	NP_000220.1:n.427+21C>G