Canonical Allele Identifier: CA2229563462

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940639_67940641delinsTCA , CM000678.2:g.67940639_67940641delinsTCA	GRCh38
NC_000016.9:g.67974542_67974544delinsTCA , CM000678.1:g.67974542_67974544delinsTCA	GRCh37
NC_000016.8:g.66532043_66532045delinsTCA	NCBI36
NG_009778.1:g.8472_8474delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-163_749-161delinsTGA MANE Select	ENSP00000264005.5:n.749-163_749-161delinsTGA
ENST00000264005.9:c.749-163_749-161delinsTGA	ENSP00000264005.5:n.749-163_749-161delinsTGA
ENST00000570369.5:c.156-567_156-565delinsTGA
ENST00000570980.1:c.533-163_533-161delinsTGA	ENSP00000464651.1:n.533-163_533-161delinsTGA
ENST00000573538.5:c.486+96_486+98delinsTGA	ENSP00000463220.1:n.486+96_486+98delinsTGA
NM_000229.1:c.749-163_749-161delinsTGA	NP_000220.1:n.749-163_749-161delinsTGA
NM_000229.2:c.749-163_749-161delinsTGA MANE Select	NP_000220.1:n.749-163_749-161delinsTGA