Canonical Allele Identifier: CA2575772206
Gene: ITGA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335889_68335890del , CM000677.2:g.68335889_68335890del GRCh38
NC_000015.9:g.68628227_68628228del , CM000677.1:g.68628227_68628228del GRCh37
NC_000015.8:g.66415281_66415282del NCBI36
NG_046911.1:g.101271_101272del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1277-45_1277-44del MANE Select ENSP00000327290.7:n.1277-45_1277-44del
ENST00000315757.8:c.1277-45_1277-44del ENSP00000327290.7:n.1277-45_1277-44del
ENST00000423218.6:c.1277-45_1277-44del ENSP00000403392.2:n.1277-45_1277-44del
ENST00000566429.1:n.197-76_197-75del
ENST00000569346.5:n.211_212del
NM_001004439.1:c.1277-45_1277-44del NP_001004439.1:n.1277-45_1277-44del
XM_005254228.2:c.971-45_971-44del XP_005254285.1:n.971-45_971-44del
XM_011521363.1:c.1070-45_1070-44del XP_011519665.1:n.1070-45_1070-44del
XM_005254228.3:c.971-45_971-44del XP_005254285.1:n.971-45_971-44del
XM_011521363.2:c.1070-45_1070-44del XP_011519665.1:n.1070-45_1070-44del
NM_001004439.2:c.1277-45_1277-44del MANE Select NP_001004439.1:n.1277-45_1277-44del