Canonical Allele Identifier: CA2322347491
Gene: ICAM1 HGNC NCBI
LIMASI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10272555_10272558delinsCTTT , CM000681.2:g.10272555_10272558delinsCTTT GRCh38
NC_000019.9:g.10383231_10383234delinsCTTT , CM000681.1:g.10383231_10383234delinsCTTT GRCh37
NC_000019.8:g.10244231_10244234delinsCTTT NCBI36
NG_012083.1:g.6715_6718delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000264832.8:c.67+1329_67+1332delinsCTTT (ICAM1) MANE Select ENSP00000264832.2:n.67+1329_67+1332delinsCTTT
ENST00000264832.7:c.67+1329_67+1332delinsCTTT (ICAM1) ENSP00000264832.2:n.67+1329_67+1332delinsCTTT
ENST00000423829.2:c.67+1329_67+1332delinsCTTT (ICAM1) ENSP00000413124.2:n.67+1329_67+1332delinsCTTT
ENST00000588645.1:c.67+1329_67+1332delinsCTTT (ICAM1) ENSP00000465680.1:n.67+1329_67+1332delinsCTTT
NM_000201.2:c.67+1329_67+1332delinsCTTT (ICAM1) NP_000192.2:n.67+1329_67+1332delinsCTTT
XR_936313.1:n.155-5764_155-5761delinsAAAG (LIMASI)
XR_936314.1:n.155-5764_155-5761delinsAAAG (LIMASI)
NM_000201.3:c.67+1329_67+1332delinsCTTT (ICAM1) MANE Select NP_000192.2:n.67+1329_67+1332delinsCTTT
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