Linked Data
ClinVar Variation Id:
198975
dbSNP Id:
rs140265039
ExAC:
14:64628890 G / A
gnomAD v2:
14-64628890-G-A
gnomAD v3:
14-64162172-G-A
gnomAD v4:
14-64162172-G-A
COSMIC:
COSM1370527
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.64162172G>A , CM000676.2:g.64162172G>A | GRCh38 |
| NC_000014.8:g.64628890G>A , CM000676.1:g.64628890G>A | GRCh37 |
| NC_000014.7:g.63698643G>A | NCBI36 |
| NG_011756.1:g.314208G>A | |
| NG_011756.2:g.405274G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555002.6:c.16195G>A (SYNE2) MANE Select | ENSP00000450831.2:p.Ala5399Thr | |
| ENST00000344113.8:c.16195G>A (SYNE2) | ENSP00000341781.4:p.Ala5399Thr | |
| ENST00000357395.7:c.15964G>A (SYNE2) | ENSP00000349969.4:p.Ala5322Thr | |
| ENST00000358025.7:c.16195G>A (SYNE2) | ENSP00000350719.3:p.Ala5399Thr | |
| ENST00000394768.6:c.5350G>A (SYNE2) | ENSP00000378249.2:p.Ala1784Thr | |
| ENST00000553289.5:c.-51G>A (SYNE2) | ENSP00000451184.1:n.-51G>A | |
| ENST00000554584.5:c.15946G>A (SYNE2) | ENSP00000452570.1:p.Ala5316Thr | |
| ENST00000555002.5:c.6097G>A (SYNE2) | ENSP00000450831.1:p.Ala2033Thr | |
| ENST00000555612.5:c.1081G>A (SYNE2) | ENSP00000451972.1:p.Ala361Thr | |
| ENST00000556275.5:c.1406+72798C>T (ESR2) | ENSP00000452485.2:n.1406+72798C>T | |
| ENST00000557024.1:n.321G>A (SYNE2) | ||
| NM_015180.4:c.16195G>A (SYNE2) | NP_055995.4:p.Ala5399Thr | |
| NM_182914.2:c.16195G>A (SYNE2) | NP_878918.2:p.Ala5399Thr | |
| XM_005267454.1:c.16195G>A (SYNE2) | XP_005267511.1:p.Ala5399Thr | |
| XM_005267456.1:c.16195G>A (SYNE2) | XP_005267513.1:p.Ala5399Thr | |
| XM_005267457.1:c.16195G>A (SYNE2) | XP_005267514.1:p.Ala5399Thr | |
| XM_005267458.1:c.16195G>A (SYNE2) | XP_005267515.1:p.Ala5399Thr | |
| XM_005267459.1:c.16195G>A (SYNE2) | XP_005267516.1:p.Ala5399Thr | |
| XM_011536574.1:c.16195G>A (SYNE2) | XP_011534876.1:p.Ala5399Thr | |
| XM_011536575.1:c.16195G>A (SYNE2) | XP_011534877.1:p.Ala5399Thr | |
| XM_011536576.1:c.16195G>A (SYNE2) | XP_011534878.1:p.Ala5399Thr | |
| XM_011536577.1:c.16195G>A (SYNE2) | XP_011534879.1:p.Ala5399Thr | |
| XM_011536578.1:c.16195G>A (SYNE2) | XP_011534880.1:p.Ala5399Thr | |
| XM_011536579.1:c.16195G>A (SYNE2) | XP_011534881.1:p.Ala5399Thr | |
| XM_011536580.1:c.16195G>A (SYNE2) | XP_011534882.1:p.Ala5399Thr | |
| XM_011536581.1:c.16195G>A (SYNE2) | XP_011534883.1:p.Ala5399Thr | |
| XM_011536582.1:c.16078G>A (SYNE2) | XP_011534884.1:p.Ala5360Thr | |
| XM_011536583.1:c.13000G>A (SYNE2) | XP_011534885.1:p.Ala4334Thr | |
| XM_011536575.2:c.16195G>A (SYNE2) | XP_011534877.1:p.Ala5399Thr | |
| XM_011536576.2:c.16195G>A (SYNE2) | XP_011534878.1:p.Ala5399Thr | |
| XM_011536577.2:c.16195G>A (SYNE2) | XP_011534879.1:p.Ala5399Thr | |
| XM_011536580.2:c.16195G>A (SYNE2) | XP_011534882.1:p.Ala5399Thr | |
| XM_017021101.1:c.16195G>A (SYNE2) | XP_016876590.1:p.Ala5399Thr | |
| XM_017021102.1:c.16126G>A (SYNE2) | XP_016876591.1:p.Ala5376Thr | |
| NM_015180.5:c.16195G>A (SYNE2) | NP_055995.4:p.Ala5399Thr | |
| NM_015180.6:c.16195G>A (SYNE2) | NP_055995.4:p.Ala5399Thr | |
| NM_182914.3:c.16195G>A (SYNE2) MANE Select | NP_878918.2:p.Ala5399Thr |