Linked Data
ClinVar Variation Id:
2017884
ClinVar RCV Id:
RCV002857101
MyVariant Identifiers:
chr17:g.7127043T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7223724T>C , CM000679.2:g.7223724T>C | GRCh38 |
| NC_000017.10:g.7127043T>C , CM000679.1:g.7127043T>C | GRCh37 |
| NC_000017.9:g.7067767T>C | NCBI36 |
| NG_007975.1:g.8891T>C | |
| NG_008391.2:g.1327A>G | |
| NG_033038.1:g.15821A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000356839.10:c.1263T>C MANE Select | ENSP00000349297.5:p.Phe421= | |
| ENST00000322910.9:c.*1218T>C | ENSP00000325395.5:n.*1218T>C | |
| ENST00000350303.9:c.1197T>C | ENSP00000344152.5:p.Phe399= | |
| ENST00000356839.9:c.1263T>C | ENSP00000349297.5:p.Phe421= | |
| ENST00000542255.6:c.121T>C | ||
| ENST00000543245.6:c.1332T>C | ENSP00000438689.2:p.Phe444= | |
| ENST00000578579.2:n.434T>C | ||
| ENST00000578711.1:n.220T>C | ||
| ENST00000578824.5:n.679T>C | ||
| ENST00000579425.5:n.287T>C | ||
| ENST00000579546.1:c.100T>C | ||
| ENST00000583850.5:n.38T>C | ||
| ENST00000583858.5:c.292T>C | ||
| ENST00000585203.6:n.471T>C | ||
| NM_000018.3:c.1263T>C | NP_000009.1:p.Phe421= | |
| NM_001033859.2:c.1197T>C | NP_001029031.1:p.Phe399= | |
| NM_001270447.1:c.1332T>C | NP_001257376.1:p.Phe444= | |
| NM_001270448.1:c.1035T>C | NP_001257377.1:p.Phe345= | |
| XM_006721516.2:c.1263T>C | XP_006721579.2:p.Phe421= | |
| XM_011523829.1:c.1263T>C | XP_011522131.1:p.Phe421= | |
| XM_011523830.1:c.1263T>C | XP_011522132.1:p.Phe421= | |
| XR_934021.1:n.1370T>C | ||
| XR_934022.1:n.1370T>C | ||
| XR_934023.1:n.1370T>C | ||
| XM_006721516.3:c.1263T>C | XP_006721579.2:p.Phe421= | |
| XM_011523829.2:c.1263T>C | XP_011522131.1:p.Phe421= | |
| XM_011523830.2:c.1263T>C | XP_011522132.1:p.Phe421= | |
| XM_024450741.1:c.1263T>C | XP_024306509.1:p.Phe421= | |
| XR_934021.2:n.1322T>C | ||
| XR_934022.2:n.1322T>C | ||
| XR_934023.2:n.1322T>C | ||
| NM_000018.4:c.1263T>C MANE Select | NP_000009.1:p.Phe421= | |
| NM_001033859.3:c.1197T>C | NP_001029031.1:p.Phe399= | |
| NM_001270447.2:c.1332T>C | NP_001257376.1:p.Phe444= | |
| NM_001270448.2:c.1035T>C | NP_001257377.1:p.Phe345= |