Canonical Allele Identifier: CA1275127607

Gene: IL1R1

Linked Data

• dbSNP Id: rs2287047

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102157594G>T , CM000664.2:g.102157594G>T	GRCh38
NC_000002.11:g.102774054G>T , CM000664.1:g.102774054G>T	GRCh37
NC_000002.10:g.102140486G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410023.6:c.-6-125G>T MANE Select	ENSP00000386380.1:n.-6-125G>T
ENST00000409288.5:c.-6-125G>T	ENSP00000386478.1:n.-6-125G>T
ENST00000409329.5:c.-6-125G>T	ENSP00000387131.1:n.-6-125G>T
ENST00000409589.5:c.-6-125G>T	ENSP00000386555.1:n.-6-125G>T
ENST00000409929.5:c.-6-125G>T	ENSP00000386776.1:n.-6-125G>T
ENST00000410023.5:c.-6-125G>T	ENSP00000386380.1:n.-6-125G>T
ENST00000413623.5:c.-6-125G>T	ENSP00000407017.1:n.-6-125G>T
ENST00000424272.5:c.-6-125G>T	ENSP00000415366.1:n.-6-125G>T
ENST00000428279.5:c.-372+3577G>T	ENSP00000410461.1:n.-372+3577G>T
ENST00000430171.1:c.-6-125G>T	ENSP00000408101.1:n.-6-125G>T
ENST00000442590.5:c.-6-125G>T	ENSP00000393296.1:n.-6-125G>T
ENST00000450319.5:c.-6-125G>T	ENSP00000411627.1:n.-6-125G>T
ENST00000452403.5:c.-6-125G>T	ENSP00000401646.1:n.-6-125G>T
NM_000877.3:c.-6-125G>T	NP_000868.1:n.-6-125G>T
NM_001288706.1:c.-6-125G>T	NP_001275635.1:n.-6-125G>T
XM_005263929.1:c.-6-125G>T	XP_005263986.1:n.-6-125G>T
XM_005263930.3:c.-6-125G>T	XP_005263987.1:n.-6-125G>T
XM_005263931.1:c.-6-125G>T	XP_005263988.1:n.-6-125G>T
XM_005263932.1:c.-6-125G>T	XP_005263989.1:n.-6-125G>T
XM_005263933.3:c.-6-125G>T	XP_005263990.1:n.-6-125G>T
XM_005263934.3:c.-6-125G>T	XP_005263991.1:n.-6-125G>T
XM_011511114.1:c.-6-125G>T	XP_011509416.1:n.-6-125G>T
XM_011511115.1:c.-6-125G>T	XP_011509417.1:n.-6-125G>T
XM_011511116.1:c.-6-125G>T	XP_011509418.1:n.-6-125G>T
XM_011511117.1:c.-6-125G>T	XP_011509419.1:n.-6-125G>T
XM_011511118.1:c.-3-128G>T	XP_011509420.1:n.-3-128G>T
XM_011511119.1:c.-542-125G>T	XP_011509421.1:n.-542-125G>T
XM_011511120.1:c.-6-125G>T	XP_011509422.1:n.-6-125G>T
NM_001320978.1:c.-6-125G>T	NP_001307907.1:n.-6-125G>T
NM_001320980.1:c.-6-125G>T	NP_001307909.1:n.-6-125G>T
NM_001320981.1:c.-6-125G>T	NP_001307910.1:n.-6-125G>T
NM_001320982.1:c.-6-125G>T	NP_001307911.1:n.-6-125G>T
NM_001320983.1:c.-372+3577G>T	NP_001307912.1:n.-372+3577G>T
NM_001320984.1:c.-365-125G>T	NP_001307913.1:n.-365-125G>T
NM_001320985.1:c.-542-125G>T	NP_001307914.1:n.-542-125G>T
NM_001320986.1:c.-6-125G>T	NP_001307915.1:n.-6-125G>T
XM_005263930.4:c.-6-125G>T	XP_005263987.1:n.-6-125G>T
XM_005263934.4:c.-6-125G>T	XP_005263991.1:n.-6-125G>T
XM_011511115.2:c.-6-125G>T	XP_011509417.1:n.-6-125G>T
XM_011511118.2:c.-3-128G>T	XP_011509420.1:n.-3-128G>T
XM_017003989.1:c.-6-125G>T	XP_016859478.1:n.-6-125G>T
NM_000877.4:c.-6-125G>T MANE Select	NP_000868.1:n.-6-125G>T
NM_001288706.2:c.-6-125G>T	NP_001275635.1:n.-6-125G>T
NM_001320978.2:c.-6-125G>T	NP_001307907.1:n.-6-125G>T
NM_001320980.2:c.-6-125G>T	NP_001307909.1:n.-6-125G>T
NM_001320981.2:c.-6-125G>T	NP_001307910.1:n.-6-125G>T
NM_001320982.2:c.-6-125G>T	NP_001307911.1:n.-6-125G>T
NM_001320986.2:c.-6-125G>T	NP_001307915.1:n.-6-125G>T