Canonical Allele Identifier: CA2807445496

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940759G>C , CM000678.2:g.67940759G>C	GRCh38
NC_000016.9:g.67974662G>C , CM000678.1:g.67974662G>C	GRCh37
NC_000016.8:g.66532163G>C	NCBI36
NG_009778.1:g.8354C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-281C>G MANE Select	ENSP00000264005.5:n.749-281C>G
ENST00000264005.9:c.749-281C>G	ENSP00000264005.5:n.749-281C>G
ENST00000570369.5:c.156-685C>G
ENST00000570980.1:c.533-281C>G	ENSP00000464651.1:n.533-281C>G
ENST00000573538.5:c.464C>G	ENSP00000463220.1:n.464C>G
NM_000229.1:c.749-281C>G	NP_000220.1:n.749-281C>G
NM_000229.2:c.749-281C>G MANE Select	NP_000220.1:n.749-281C>G