Linked Data
dbSNP Id:
rs766650660
gnomAD v2:
16-16249167-C-CTAT
gnomAD v3:
16-16155310-C-CTAT
gnomAD v4:
16-16155310-C-CTAT
MyVariant Identifiers:
chr16:g.16249167_16249168insTAT (hg19)
chr16:g.16155310_16155311insTAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16155312_16155314dup , CM000678.2:g.16155312_16155314dup | GRCh38 |
| NC_000016.9:g.16249169_16249171dup , CM000678.1:g.16249169_16249171dup | GRCh37 |
| NC_000016.8:g.16156670_16156672dup | NCBI36 |
| NG_007558.2:g.73159_73161dup | |
| NG_007558.3:g.73305_73307dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000576204.6:n.464_466dup | ||
| ENST00000622290.5:c.*55-282_*55-280dup | ENSP00000483331.2:n.*55-282_*55-280dup | |
| ENST00000205557.12:c.3883-282_3883-280dup MANE Select | ENSP00000205557.7:n.3883-282_3883-280dup | |
| ENST00000640696.1:c.697-282_697-280dup | ENSP00000492197.1:n.697-282_697-280dup | |
| ENST00000205557.11:c.3883-282_3883-280dup | ENSP00000205557.7:n.3883-282_3883-280dup | |
| ENST00000456970.6:c.3508-282_3508-280dup | ENSP00000405002.2:n.3508-282_3508-280dup | |
| ENST00000576204.5:n.464_466dup | ||
| ENST00000622290.4:c.*1092-282_*1092-280dup | ENSP00000483331.1:n.*1092-282_*1092-280dup | |
| NM_001171.5:c.3883-282_3883-280dup | NP_001162.4:n.3883-282_3883-280dup | |
| XM_011522479.1:c.3850-282_3850-280dup | XP_011520781.1:n.3850-282_3850-280dup | |
| XM_011522480.1:c.3541-282_3541-280dup | XP_011520782.1:n.3541-282_3541-280dup | |
| XM_011522481.1:c.3541-282_3541-280dup | XP_011520783.1:n.3541-282_3541-280dup | |
| XR_932836.1:n.4181-282_4181-280dup | ||
| XR_932837.1:n.3919-282_3919-280dup | ||
| XR_932838.1:n.3982-282_3982-280dup | ||
| XR_933134.1:n.539-4469_539-4467dup | ||
| NM_001351800.1:c.3541-282_3541-280dup | NP_001338729.1:n.3541-282_3541-280dup | |
| NR_147784.1:n.3545-282_3545-280dup | ||
| XM_011522479.2:c.3850-282_3850-280dup | XP_011520781.1:n.3850-282_3850-280dup | |
| XM_011522481.3:c.3541-282_3541-280dup | XP_011520783.1:n.3541-282_3541-280dup | |
| XM_017023212.1:c.3715-282_3715-280dup | XP_016878701.1:n.3715-282_3715-280dup | |
| XM_024450261.1:c.3919-282_3919-280dup | XP_024306029.1:n.3919-282_3919-280dup | |
| XR_932836.2:n.4127-282_4127-280dup | ||
| XR_932837.3:n.3864-282_3864-280dup | ||
| XR_932838.3:n.3927-282_3927-280dup | ||
| NM_001171.6:c.3883-282_3883-280dup MANE Select | NP_001162.5:n.3883-282_3883-280dup |