Canonical Allele Identifier: CA2575772204
Gene: ITGA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335868G>A , CM000677.2:g.68335868G>A GRCh38
NC_000015.9:g.68628206G>A , CM000677.1:g.68628206G>A GRCh37
NC_000015.8:g.66415260G>A NCBI36
NG_046911.1:g.101293C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1277-23C>T MANE Select ENSP00000327290.7:n.1277-23C>T
ENST00000315757.8:c.1277-23C>T ENSP00000327290.7:n.1277-23C>T
ENST00000423218.6:c.1277-23C>T ENSP00000403392.2:n.1277-23C>T
ENST00000566429.1:n.197-54C>T
ENST00000569346.5:n.233C>T
NM_001004439.1:c.1277-23C>T NP_001004439.1:n.1277-23C>T
XM_005254228.2:c.971-23C>T XP_005254285.1:n.971-23C>T
XM_011521363.1:c.1070-23C>T XP_011519665.1:n.1070-23C>T
XM_005254228.3:c.971-23C>T XP_005254285.1:n.971-23C>T
XM_011521363.2:c.1070-23C>T XP_011519665.1:n.1070-23C>T
NM_001004439.2:c.1277-23C>T MANE Select NP_001004439.1:n.1277-23C>T