Canonical Allele Identifier: CA2184934391
Gene: ITGA11 HGNC NCBI

Linked Data

dbSNP Id: rs1595865268
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335866C>T , CM000677.2:g.68335866C>T GRCh38
NC_000015.9:g.68628204C>T , CM000677.1:g.68628204C>T GRCh37
NC_000015.8:g.66415258C>T NCBI36
NG_046911.1:g.101295G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1277-21G>A MANE Select ENSP00000327290.7:n.1277-21G>A
ENST00000315757.8:c.1277-21G>A ENSP00000327290.7:n.1277-21G>A
ENST00000423218.6:c.1277-21G>A ENSP00000403392.2:n.1277-21G>A
ENST00000566429.1:n.197-52G>A
ENST00000569346.5:n.235G>A
NM_001004439.1:c.1277-21G>A NP_001004439.1:n.1277-21G>A
XM_005254228.2:c.971-21G>A XP_005254285.1:n.971-21G>A
XM_011521363.1:c.1070-21G>A XP_011519665.1:n.1070-21G>A
XM_005254228.3:c.971-21G>A XP_005254285.1:n.971-21G>A
XM_011521363.2:c.1070-21G>A XP_011519665.1:n.1070-21G>A
NM_001004439.2:c.1277-21G>A MANE Select NP_001004439.1:n.1277-21G>A
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