Canonical Allele Identifier: CA2629178906
Gene: ITGA11 HGNC NCBI

Linked Data

gnomAD v4: 15-68335915-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335915G>T , CM000677.2:g.68335915G>T GRCh38
NC_000015.9:g.68628253G>T , CM000677.1:g.68628253G>T GRCh37
NC_000015.8:g.66415307G>T NCBI36
NG_046911.1:g.101246C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1277-70C>A MANE Select ENSP00000327290.7:n.1277-70C>A
ENST00000315757.8:c.1277-70C>A ENSP00000327290.7:n.1277-70C>A
ENST00000423218.6:c.1277-70C>A ENSP00000403392.2:n.1277-70C>A
ENST00000566429.1:n.197-101C>A
ENST00000569346.5:n.186C>A
NM_001004439.1:c.1277-70C>A NP_001004439.1:n.1277-70C>A
XM_005254228.2:c.971-70C>A XP_005254285.1:n.971-70C>A
XM_011521363.1:c.1070-70C>A XP_011519665.1:n.1070-70C>A
XM_005254228.3:c.971-70C>A XP_005254285.1:n.971-70C>A
XM_011521363.2:c.1070-70C>A XP_011519665.1:n.1070-70C>A
NM_001004439.2:c.1277-70C>A MANE Select NP_001004439.1:n.1277-70C>A
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