Canonical Allele Identifier: CA2539165722

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940594dup , CM000678.2:g.67940594dup	GRCh38
NC_000016.9:g.67974497dup , CM000678.1:g.67974497dup	GRCh37
NC_000016.8:g.66531998dup	NCBI36
NG_009778.1:g.8519dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-116dup MANE Select	ENSP00000264005.5:n.749-116dup
ENST00000264005.9:c.749-116dup	ENSP00000264005.5:n.749-116dup
ENST00000570369.5:c.156-520dup
ENST00000570980.1:c.533-116dup	ENSP00000464651.1:n.533-116dup
ENST00000573538.5:c.487-116dup	ENSP00000463220.1:n.487-116dup
NM_000229.1:c.749-116dup	NP_000220.1:n.749-116dup
NM_000229.2:c.749-116dup MANE Select	NP_000220.1:n.749-116dup