Canonical Allele Identifier: CA631724332

Gene: ICAM1 LIMASI

Linked Data

• dbSNP Id: rs1487212866
• gnomAD v2: 19-10383188-TCTGAGGGAC-T
• MyVariant Identifiers: chr19:g.10383189_10383197del (hg19) ; chr19:g.10272513_10272521del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10272517_10272525del , CM000681.2:g.10272517_10272525del	GRCh38
NC_000019.9:g.10383193_10383201del , CM000681.1:g.10383193_10383201del	GRCh37
NC_000019.8:g.10244193_10244201del	NCBI36
NG_012083.1:g.6677_6685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264832.8:c.67+1291_67+1299del (ICAM1) MANE Select	ENSP00000264832.2:n.67+1291_67+1299del
ENST00000264832.7:c.67+1291_67+1299del (ICAM1)	ENSP00000264832.2:n.67+1291_67+1299del
ENST00000423829.2:c.67+1291_67+1299del (ICAM1)	ENSP00000413124.2:n.67+1291_67+1299del
ENST00000588645.1:c.67+1291_67+1299del (ICAM1)	ENSP00000465680.1:n.67+1291_67+1299del
NM_000201.2:c.67+1291_67+1299del (ICAM1)	NP_000192.2:n.67+1291_67+1299del
XR_936313.1:n.155-5727_155-5719del (LIMASI)
XR_936314.1:n.155-5727_155-5719del (LIMASI)
NM_000201.3:c.67+1291_67+1299del (ICAM1) MANE Select	NP_000192.2:n.67+1291_67+1299del