Canonical Allele Identifier: CA2229564637

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942985_67942986delinsCG , CM000678.2:g.67942985_67942986delinsCG	GRCh38
NC_000016.9:g.67976888_67976889delinsCG , CM000678.1:g.67976888_67976889delinsCG	GRCh37
NC_000016.8:g.66534389_66534390delinsCG	NCBI36
NG_009778.1:g.6127_6128delinsCG
NG_033098.1:g.30709_30710delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.312-10_312-9delinsCG MANE Select	ENSP00000264005.5:n.312-10_312-9delinsCG
ENST00000264005.9:c.312-10_312-9delinsCG	ENSP00000264005.5:n.312-10_312-9delinsCG
ENST00000570369.5:c.40-10_40-9delinsCG
ENST00000570980.1:c.96-10_96-9delinsCG	ENSP00000464651.1:n.96-10_96-9delinsCG
ENST00000575277.1:n.90-10_90-9delinsCG
ENST00000575467.5:c.*7-10_*7-9delinsCG	ENSP00000460653.1:n.*7-10_*7-9delinsCG
NM_000229.1:c.312-10_312-9delinsCG	NP_000220.1:n.312-10_312-9delinsCG
NM_000229.2:c.312-10_312-9delinsCG MANE Select	NP_000220.1:n.312-10_312-9delinsCG