Canonical Allele Identifier: CA622937062
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1188151330
gnomAD v2: 16-67974738-CAA-C
gnomAD v3: 16-67940835-CAA-C
gnomAD v4: 16-67940835-CAA-C
MyVariant Identifiers: chr16:g.67974740_67974741del (hg19) chr16:g.67974739_67974740del (hg19) chr16:g.67940836_67940837del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940854_67940855del , CM000678.2:g.67940854_67940855del GRCh38
NC_000016.9:g.67974757_67974758del , CM000678.1:g.67974757_67974758del GRCh37
NC_000016.8:g.66532258_66532259del NCBI36
NG_009778.1:g.8276_8277del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-359_749-358del MANE Select ENSP00000264005.5:n.749-359_749-358del
ENST00000264005.9:c.749-359_749-358del ENSP00000264005.5:n.749-359_749-358del
ENST00000570369.5:c.156-763_156-762del
ENST00000570980.1:c.533-359_533-358del ENSP00000464651.1:n.533-359_533-358del
ENST00000573538.5:c.392-6_392-5del ENSP00000463220.1:n.392-6_392-5del
NM_000229.1:c.749-359_749-358del NP_000220.1:n.749-359_749-358del
NM_000229.2:c.749-359_749-358del MANE Select NP_000220.1:n.749-359_749-358del
Search 100 bp 5'
Search 100 bp 3'