Canonical Allele Identifier: CA993450639
Gene: ICAM1 HGNC NCBI
LIMASI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10272559_10272560insTTTTTTTTTTTTT , CM000681.2:g.10272559_10272560insTTTTTTTTTTTTT GRCh38
NC_000019.9:g.10383235_10383236insTTTTTTTTTTTTT , CM000681.1:g.10383235_10383236insTTTTTTTTTTTTT GRCh37
NC_000019.8:g.10244235_10244236insTTTTTTTTTTTTT NCBI36
NG_012083.1:g.6719_6720insTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264832.8:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) MANE Select ENSP00000264832.2:n.67+1333_67+1334insTTTTTTTTTTTTT
ENST00000264832.7:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) ENSP00000264832.2:n.67+1333_67+1334insTTTTTTTTTTTTT
ENST00000423829.2:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) ENSP00000413124.2:n.67+1333_67+1334insTTTTTTTTTTTTT
ENST00000588645.1:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) ENSP00000465680.1:n.67+1333_67+1334insTTTTTTTTTTTTT
NM_000201.2:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) NP_000192.2:n.67+1333_67+1334insTTTTTTTTTTTTT
XR_936313.1:n.155-5762_155-5761insAAAAAAAAAAAAA (LIMASI)
XR_936314.1:n.155-5762_155-5761insAAAAAAAAAAAAA (LIMASI)
NM_000201.3:c.67+1333_67+1334insTTTTTTTTTTTTT (ICAM1) MANE Select NP_000192.2:n.67+1333_67+1334insTTTTTTTTTTTTT