Linked Data
dbSNP Id:
rs1726026953
gnomAD v2:
4-102740054-C-CTTTTT
gnomAD v3:
4-101818897-C-CTTTTT
gnomAD v4:
4-101818897-C-CTTTTT
MyVariant Identifiers:
chr4:g.102740054_102740055insTTTTT (hg19)
chr4:g.101818897_101818898insTTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.101818898_101818899insTTTTT , CM000666.2:g.101818898_101818899insTTTTT | GRCh38 |
| NC_000004.11:g.102740055_102740056insTTTTT , CM000666.1:g.102740055_102740056insTTTTT | GRCh37 |
| NC_000004.10:g.102959078_102959079insTTTTT | NCBI36 |
| NG_015824.1:g.33292_33293insTTTTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322953.9:c.71-10910_71-10909insTTTTT MANE Select | ENSP00000320509.4:n.71-10910_71-10909insTTTTT | |
| ENST00000322953.8:c.71-10910_71-10909insTTTTT | ENSP00000320509.4:n.71-10910_71-10909insTTTTT | |
| ENST00000428908.5:c.70+27948_70+27949insTTTTT | ENSP00000412748.1:n.70+27948_70+27949insTTTTT | |
| ENST00000444316.2:c.-21+4960_-21+4961insTTTTT | ENSP00000388817.2:n.-21+4960_-21+4961insTTTTT | |
| ENST00000504592.5:c.26-10910_26-10909insTTTTT | ENSP00000421443.1:n.26-10910_26-10909insTTTTT | |
| ENST00000508653.5:c.70+27948_70+27949insTTTTT | ENSP00000422314.1:n.70+27948_70+27949insTTTTT | |
| NM_001083907.2:c.-21+4960_-21+4961insTTTTT | NP_001077376.2:n.-21+4960_-21+4961insTTTTT | |
| NM_001127507.2:c.70+27948_70+27949insTTTTT | NP_001120979.2:n.70+27948_70+27949insTTTTT | |
| NM_017935.4:c.71-10910_71-10909insTTTTT | NP_060405.4:n.71-10910_71-10909insTTTTT | |
| XM_017008337.2:c.-20-10910_-20-10909insTTTTT | XP_016863826.1:n.-20-10910_-20-10909insTTTTT | |
| NM_017935.5:c.71-10910_71-10909insTTTTT MANE Select | NP_060405.5:n.71-10910_71-10909insTTTTT | |
| NM_001083907.3:c.-21+4960_-21+4961insTTTTT | NP_001077376.3:n.-21+4960_-21+4961insTTTTT | |
| NM_001127507.3:c.70+27948_70+27949insTTTTT | NP_001120979.3:n.70+27948_70+27949insTTTTT |