Canonical Allele Identifier: CA631724350

Gene: ICAM1 LIMASI

Linked Data

• dbSNP Id: rs1359010923
• gnomAD v2: 19-10383239-T-TTC
• gnomAD v3: 19-10272563-T-TTC
• gnomAD v4: 19-10272563-T-TTC
• MyVariant Identifiers: chr19:g.10383239_10383240insTC (hg19) ; chr19:g.10272563_10272564insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10272564_10272565insCT , CM000681.2:g.10272564_10272565insCT	GRCh38
NC_000019.9:g.10383240_10383241insCT , CM000681.1:g.10383240_10383241insCT	GRCh37
NC_000019.8:g.10244240_10244241insCT	NCBI36
NG_012083.1:g.6724_6725insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264832.8:c.67+1338_67+1339insCT (ICAM1) MANE Select	ENSP00000264832.2:n.67+1338_67+1339insCT
ENST00000264832.7:c.67+1338_67+1339insCT (ICAM1)	ENSP00000264832.2:n.67+1338_67+1339insCT
ENST00000423829.2:c.67+1338_67+1339insCT (ICAM1)	ENSP00000413124.2:n.67+1338_67+1339insCT
ENST00000588645.1:c.67+1338_67+1339insCT (ICAM1)	ENSP00000465680.1:n.67+1338_67+1339insCT
NM_000201.2:c.67+1338_67+1339insCT (ICAM1)	NP_000192.2:n.67+1338_67+1339insCT
XR_936313.1:n.155-5770_155-5769insGA (LIMASI)
XR_936314.1:n.155-5770_155-5769insGA (LIMASI)
NM_000201.3:c.67+1338_67+1339insCT (ICAM1) MANE Select	NP_000192.2:n.67+1338_67+1339insCT