Canonical Allele Identifier: CA2184934354

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335780_68335807delinsACCGGGGGGCTCCGGCCACGTACACCCG , CM000677.2:g.68335780_68335807delinsACCGGGGGGCTCCGGCCACGTACACCCG	GRCh38
NC_000015.9:g.68628118_68628145delinsACCGGGGGGCTCCGGCCACGTACACCCG , CM000677.1:g.68628118_68628145delinsACCGGGGGGCTCCGGCCACGTACACCCG	GRCh37
NC_000015.8:g.66415172_66415199delinsACCGGGGGGCTCCGGCCACGTACACCCG	NCBI36
NG_046911.1:g.101354_101381delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1315_1342delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT MANE Select	ENSP00000327290.7:p.Arg439=
ENST00000315757.8:c.1315_1342delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	ENSP00000327290.7:p.Arg439=
ENST00000423218.6:c.1315_1342delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	ENSP00000403392.2:p.Arg439=
ENST00000566429.1:n.204_231delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT
ENST00000569346.5:n.294_321delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT
NM_001004439.1:c.1315_1342delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	NP_001004439.1:p.Arg439=
XM_005254228.2:c.1009_1036delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	XP_005254285.1:p.Arg337=
XM_011521363.1:c.1108_1135delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	XP_011519665.1:p.Arg370=
XM_005254228.3:c.1009_1036delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	XP_005254285.1:p.Arg337=
XM_011521363.2:c.1108_1135delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT	XP_011519665.1:p.Arg370=
NM_001004439.2:c.1315_1342delinsCGGGTGTACGTGGCCGGAGCCCCCCGGT MANE Select	NP_001004439.1:p.Arg439=