Canonical Allele Identifier: CA2807445495

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940736C>A , CM000678.2:g.67940736C>A	GRCh38
NC_000016.9:g.67974639C>A , CM000678.1:g.67974639C>A	GRCh37
NC_000016.8:g.66532140C>A	NCBI36
NG_009778.1:g.8377G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-258G>T MANE Select	ENSP00000264005.5:n.749-258G>T
ENST00000264005.9:c.749-258G>T	ENSP00000264005.5:n.749-258G>T
ENST00000570369.5:c.156-662G>T
ENST00000570980.1:c.533-258G>T	ENSP00000464651.1:n.533-258G>T
ENST00000573538.5:c.486+1G>T	ENSP00000463220.1:n.486+1G>T
NM_000229.1:c.749-258G>T	NP_000220.1:n.749-258G>T
NM_000229.2:c.749-258G>T MANE Select	NP_000220.1:n.749-258G>T