Canonical Allele Identifier: CA2229564548

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942788_67942789delinsCG , CM000678.2:g.67942788_67942789delinsCG	GRCh38
NC_000016.9:g.67976691_67976692delinsCG , CM000678.1:g.67976691_67976692delinsCG	GRCh37
NC_000016.8:g.66534192_66534193delinsCG	NCBI36
NG_009778.1:g.6324_6325delinsCG
NG_033098.1:g.30906_30907delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-23_428-22delinsCG MANE Select	ENSP00000264005.5:n.428-23_428-22delinsCG
ENST00000264005.9:c.428-23_428-22delinsCG	ENSP00000264005.5:n.428-23_428-22delinsCG
ENST00000570369.5:c.155+72_155+73delinsCG
ENST00000570980.1:c.212-23_212-22delinsCG	ENSP00000464651.1:n.212-23_212-22delinsCG
ENST00000573538.5:c.71-23_71-22delinsCG	ENSP00000463220.1:n.71-23_71-22delinsCG
ENST00000573846.1:n.42-23_42-22delinsCG
ENST00000575277.1:n.206-23_206-22delinsCG
ENST00000575467.5:c.*123-23_*123-22delinsCG	ENSP00000460653.1:n.*123-23_*123-22delinsCG
NM_000229.1:c.428-23_428-22delinsCG	NP_000220.1:n.428-23_428-22delinsCG
NM_000229.2:c.428-23_428-22delinsCG MANE Select	NP_000220.1:n.428-23_428-22delinsCG