Canonical Allele Identifier: CA2229563450

Gene: LCAT

Linked Data

• dbSNP Id: rs2058286776

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940616del , CM000678.2:g.67940616del	GRCh38
NC_000016.9:g.67974519del , CM000678.1:g.67974519del	GRCh37
NC_000016.8:g.66532020del	NCBI36
NG_009778.1:g.8497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-138del MANE Select	ENSP00000264005.5:n.749-138del
ENST00000264005.9:c.749-138del	ENSP00000264005.5:n.749-138del
ENST00000570369.5:c.156-542del
ENST00000570980.1:c.533-138del	ENSP00000464651.1:n.533-138del
ENST00000573538.5:c.486+121del	ENSP00000463220.1:n.486+121del
NM_000229.1:c.749-138del	NP_000220.1:n.749-138del
NM_000229.2:c.749-138del MANE Select	NP_000220.1:n.749-138del