Canonical Allele Identifier: CA622937058
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1163822071
gnomAD v2: 16-67974736-T-TA
gnomAD v3: 16-67940833-T-TA
gnomAD v4: 16-67940833-T-TA
MyVariant Identifiers: chr16:g.67974738delinsAC (hg19) chr16:g.67974736_67974737insA (hg19) chr16:g.67940833_67940834insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940834dup , CM000678.2:g.67940834dup GRCh38
NC_000016.9:g.67974737dup , CM000678.1:g.67974737dup GRCh37
NC_000016.8:g.66532238dup NCBI36
NG_009778.1:g.8279dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-356dup MANE Select ENSP00000264005.5:n.749-356dup
ENST00000264005.9:c.749-356dup ENSP00000264005.5:n.749-356dup
ENST00000570369.5:c.156-760dup
ENST00000570980.1:c.533-356dup ENSP00000464651.1:n.533-356dup
ENST00000573538.5:c.392-3dup ENSP00000463220.1:n.392-3dup
NM_000229.1:c.749-356dup NP_000220.1:n.749-356dup
NM_000229.2:c.749-356dup MANE Select NP_000220.1:n.749-356dup
Search 100 bp 5'
Search 100 bp 3'