Canonical Allele Identifier: CA783150668

Gene: ICAM1 LIMASI

Linked Data

• dbSNP Id: rs1174775027
• gnomAD v3: 19-10272560-CTTTTT-C
• gnomAD v4: 19-10272560-CTTTTT-C
• MyVariant Identifiers: chr19:g.10383237_10383241del (hg19) ; chr19:g.10272561_10272565del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10272578_10272582del , CM000681.2:g.10272578_10272582del	GRCh38
NC_000019.9:g.10383254_10383258del , CM000681.1:g.10383254_10383258del	GRCh37
NC_000019.8:g.10244254_10244258del	NCBI36
NG_012083.1:g.6738_6742del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264832.8:c.67+1352_67+1356del (ICAM1) MANE Select	ENSP00000264832.2:n.67+1352_67+1356del
ENST00000264832.7:c.67+1352_67+1356del (ICAM1)	ENSP00000264832.2:n.67+1352_67+1356del
ENST00000423829.2:c.67+1352_67+1356del (ICAM1)	ENSP00000413124.2:n.67+1352_67+1356del
ENST00000588645.1:c.67+1352_67+1356del (ICAM1)	ENSP00000465680.1:n.67+1352_67+1356del
NM_000201.2:c.67+1352_67+1356del (ICAM1)	NP_000192.2:n.67+1352_67+1356del
XR_936313.1:n.155-5771_155-5767del (LIMASI)
XR_936314.1:n.155-5771_155-5767del (LIMASI)
NM_000201.3:c.67+1352_67+1356del (ICAM1) MANE Select	NP_000192.2:n.67+1352_67+1356del