Canonical Allele Identifier: CA919730875

Gene: LCAT

Linked Data

• dbSNP Id: rs1567409114
• gnomAD v3: 16-67942788-CG-C
• gnomAD v4: 16-67942788-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942793del , CM000678.2:g.67942793del	GRCh38
NC_000016.9:g.67976696del , CM000678.1:g.67976696del	GRCh37
NC_000016.8:g.66534197del	NCBI36
NG_009778.1:g.6324del
NG_033098.1:g.30906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-23del MANE Select	ENSP00000264005.5:n.428-23del
ENST00000264005.9:c.428-23del	ENSP00000264005.5:n.428-23del
ENST00000570369.5:c.155+72del
ENST00000570980.1:c.212-23del	ENSP00000464651.1:n.212-23del
ENST00000573538.5:c.71-23del	ENSP00000463220.1:n.71-23del
ENST00000573846.1:n.42-23del
ENST00000575277.1:n.206-23del
ENST00000575467.5:c.*123-23del	ENSP00000460653.1:n.*123-23del
NM_000229.1:c.428-23del	NP_000220.1:n.428-23del
NM_000229.2:c.428-23del MANE Select	NP_000220.1:n.428-23del