Canonical Allele Identifier: CA783150690

Gene: ICAM1 LIMASI

Linked Data

• dbSNP Id: rs1314080278
• gnomAD v3: 19-10272565-T-TTC
• gnomAD v4: 19-10272565-T-TTC
• MyVariant Identifiers: chr19:g.10383241_10383242insTC (hg19) ; chr19:g.10272565_10272566insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10272566_10272567insCT , CM000681.2:g.10272566_10272567insCT	GRCh38
NC_000019.9:g.10383242_10383243insCT , CM000681.1:g.10383242_10383243insCT	GRCh37
NC_000019.8:g.10244242_10244243insCT	NCBI36
NG_012083.1:g.6726_6727insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264832.8:c.67+1340_67+1341insCT (ICAM1) MANE Select	ENSP00000264832.2:n.67+1340_67+1341insCT
ENST00000264832.7:c.67+1340_67+1341insCT (ICAM1)	ENSP00000264832.2:n.67+1340_67+1341insCT
ENST00000423829.2:c.67+1340_67+1341insCT (ICAM1)	ENSP00000413124.2:n.67+1340_67+1341insCT
ENST00000588645.1:c.67+1340_67+1341insCT (ICAM1)	ENSP00000465680.1:n.67+1340_67+1341insCT
NM_000201.2:c.67+1340_67+1341insCT (ICAM1)	NP_000192.2:n.67+1340_67+1341insCT
XR_936313.1:n.155-5772_155-5771insGA (LIMASI)
XR_936314.1:n.155-5772_155-5771insGA (LIMASI)
NM_000201.3:c.67+1340_67+1341insCT (ICAM1) MANE Select	NP_000192.2:n.67+1340_67+1341insCT