Canonical Allele Identifier: CA783150585

Gene: ICAM1 LIMASI

Linked Data

• dbSNP Id: rs1276326819
• gnomAD v3: 19-10272539-CTTCT-C
• gnomAD v4: 19-10272539-CTTCT-C
• MyVariant Identifiers: chr19:g.10383216_10383219del (hg19) ; chr19:g.10272540_10272543del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10272550_10272553del , CM000681.2:g.10272550_10272553del	GRCh38
NC_000019.9:g.10383226_10383229del , CM000681.1:g.10383226_10383229del	GRCh37
NC_000019.8:g.10244226_10244229del	NCBI36
NG_012083.1:g.6710_6713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264832.8:c.67+1324_67+1327del (ICAM1) MANE Select	ENSP00000264832.2:n.67+1324_67+1327del
ENST00000264832.7:c.67+1324_67+1327del (ICAM1)	ENSP00000264832.2:n.67+1324_67+1327del
ENST00000423829.2:c.67+1324_67+1327del (ICAM1)	ENSP00000413124.2:n.67+1324_67+1327del
ENST00000588645.1:c.67+1324_67+1327del (ICAM1)	ENSP00000465680.1:n.67+1324_67+1327del
NM_000201.2:c.67+1324_67+1327del (ICAM1)	NP_000192.2:n.67+1324_67+1327del
XR_936313.1:n.155-5749_155-5746del (LIMASI)
XR_936314.1:n.155-5749_155-5746del (LIMASI)
NM_000201.3:c.67+1324_67+1327del (ICAM1) MANE Select	NP_000192.2:n.67+1324_67+1327del