Canonical Allele Identifier: CA641153688

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs778228325
• gnomAD v2: X-29935791-ATTTT-A
• gnomAD v3: X-29917674-ATTTT-A
• gnomAD v4: X-29917674-ATTTT-A
• MyVariant Identifiers: chrX:g.29935792_29935795del (hg19) ; chrX:g.29917675_29917678del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917680_29917683del , CM000685.2:g.29917680_29917683del	GRCh38
NC_000023.10:g.29935797_29935800del , CM000685.1:g.29935797_29935800del	GRCh37
NC_000023.9:g.29845718_29845721del	NCBI36
NG_008292.1:g.1335117_1335120del
NG_008292.2:g.1335117_1335120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.911+84_911+87del MANE Select	ENSP00000368278.1:n.911+84_911+87del
ENST00000302196.5:c.134+84_134+87del	ENSP00000305200.5:n.134+84_134+87del
ENST00000378993.5:c.911+84_911+87del	ENSP00000368278.1:n.911+84_911+87del
NM_014271.3:c.911+84_911+87del	NP_055086.1:n.911+84_911+87del
XM_005274441.1:c.911+84_911+87del	XP_005274498.1:n.911+84_911+87del
XM_011545445.1:c.911+84_911+87del	XP_011543747.1:n.911+84_911+87del
XM_017029240.1:c.911+84_911+87del	XP_016884729.1:n.911+84_911+87del
XM_017029241.1:c.533+84_533+87del	XP_016884730.1:n.533+84_533+87del
NM_014271.4:c.911+84_911+87del MANE Select	NP_055086.1:n.911+84_911+87del