Canonical Allele Identifier: CA344175
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs267606574

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490412_67490414del , CM000673.2:g.67490412_67490414del GRCh38
NC_000011.9:g.67257883_67257885del , CM000673.1:g.67257883_67257885del GRCh37
NC_000011.8:g.67014459_67014461del NCBI36
NG_008969.1:g.12379_12381del , LRG_460:g.12379_12381del

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.719_721del
ENST00000528641.7:c.553_555del ENSP00000434982.3:p.Tyr185del
ENST00000529797.2:n.1254_1256del
ENST00000682324.1:c.469-585_469-583del ENSP00000508017.1:n.469-585_469-583del
ENST00000682659.1:c.373_375del ENSP00000507351.1:p.Tyr125del
ENST00000682699.1:c.742_744del ENSP00000507935.1:p.Tyr248del
ENST00000683237.1:c.742_744del ENSP00000507343.1:p.Tyr248del
ENST00000683856.1:c.565_567del ENSP00000507979.1:p.Tyr189del
ENST00000684006.1:c.742_744del ENSP00000507269.1:p.Tyr248del
ENST00000684657.1:c.562_564del ENSP00000507961.1:p.Tyr188del
ENST00000279146.8:c.742_744del MANE Select ENSP00000279146.3:p.Tyr248del
ENST00000279146.7:c.742_744del ENSP00000279146.3:p.Tyr248del
ENST00000525341.1:c.394_396del ENSP00000476993.1:p.Tyr132del
ENST00000528641.6:c.553_555del ENSP00000434982.2:p.Tyr185del
NM_001302959.1:c.565_567del NP_001289888.1:p.Tyr189del
NM_001302960.1:c.742_744del NP_001289889.1:p.Tyr248del
NM_003977.3:c.742_744del NP_003968.3:p.Tyr248del
XM_024448761.1:c.742_744del XP_024304529.1:p.Tyr248del
NM_003977.4:c.742_744del MANE Select NP_003968.3:p.Tyr248del
NM_001302960.2:c.742_744del NP_001289889.1:p.Tyr248del
NM_001302959.2:c.565_567del NP_001289888.1:p.Tyr189del