Linked Data
ClinVar Variation Id:
185249
dbSNP Id:
rs786202031
MyVariant Identifiers:
chr13:g.32912902_32912904delinsCAT (hg19)
chr13:g.32338765_32338767delinsCAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32338765_32338767delinsCAT , CM000675.2:g.32338765_32338767delinsCAT | GRCh38 |
| NC_000013.10:g.32912902_32912904delinsCAT , CM000675.1:g.32912902_32912904delinsCAT | GRCh37 |
| NC_000013.9:g.31810902_31810904delinsCAT | NCBI36 |
| NG_012772.3:g.28286_28288delinsCAT , LRG_293:g.28286_28288delinsCAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.4410_4412delinsCAT | ENSP00000434898.2:p.Arg1471Ile | |
| ENST00000528762.2:c.4410_4412delinsCAT | ENSP00000433168.2:p.Arg1471Ile | |
| ENST00000530893.7:c.4041_4043delinsCAT | ENSP00000499438.2:p.Arg1348Ile | |
| ENST00000665585.2:c.4410_4412delinsCAT | ENSP00000499570.2:p.Arg1471Ile | |
| ENST00000666593.2:c.4410_4412delinsCAT | ENSP00000499256.2:p.Arg1471Ile | |
| ENST00000700202.2:c.4410_4412delinsCAT | ENSP00000514856.2:p.Arg1471Ile | |
| ENST00000380152.8:c.4410_4412delinsCAT MANE Select | ENSP00000369497.3:p.Arg1471Ile | |
| ENST00000544455.6:c.4410_4412delinsCAT | ENSP00000439902.1:p.Arg1471Ile | |
| ENST00000614259.2:c.4410_4412delinsCAT | ENSP00000506251.1:p.Arg1471Ile | |
| ENST00000680887.1:c.4410_4412delinsCAT | ENSP00000505508.1:p.Arg1471Ile | |
| ENST00000380152.7:c.4410_4412delinsCAT | ENSP00000369497.3:p.Arg1471Ile | |
| ENST00000544455.5:c.4410_4412delinsCAT | ENSP00000439902.1:p.Arg1471Ile | |
| ENST00000614259.1:n.4410_4412delinsCAT | ||
| NM_000059.3:c.4410_4412delinsCAT , LRG_293t1:c.4410_4412delinsCAT | NP_000050.2:p.Arg1471Ile | |
| XM_011535203.1:c.4410_4412delinsCAT | XP_011533505.1:p.Arg1471Ile | |
| XM_011535204.1:c.4410_4412delinsCAT | XP_011533506.1:p.Arg1471Ile | |
| XM_011535205.1:c.4410_4412delinsCAT | XP_011533507.1:p.Arg1471Ile | |
| NM_000059.4:c.4410_4412delinsCAT MANE Select | NP_000050.3:p.Arg1471Ile |