Linked Data
ClinVar Variation Id:
282103
dbSNP Id:
rs141051652
ExAC:
14:64676722 G / A
gnomAD v2:
14-64676722-G-A
gnomAD v3:
14-64210004-G-A
gnomAD v4:
14-64210004-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.64210004G>A , CM000676.2:g.64210004G>A | GRCh38 |
| NC_000014.8:g.64676722G>A , CM000676.1:g.64676722G>A | GRCh37 |
| NC_000014.7:g.63746475G>A | NCBI36 |
| NG_011756.1:g.362040G>A | |
| NG_011756.2:g.453106G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554805.6:n.522G>A (SYNE2) | ||
| ENST00000555002.6:c.18603G>A (SYNE2) MANE Select | ENSP00000450831.2:p.Arg6201= | |
| ENST00000344113.8:c.18603G>A (SYNE2) | ENSP00000341781.4:p.Arg6201= | |
| ENST00000357395.7:c.18498G>A (SYNE2) | ENSP00000349969.4:p.Arg6166= | |
| ENST00000358025.7:c.18603G>A (SYNE2) | ENSP00000350719.3:p.Arg6201= | |
| ENST00000394768.6:c.7758G>A (SYNE2) | ENSP00000378249.2:p.Arg2586= | |
| ENST00000553289.5:c.*478G>A (SYNE2) | ENSP00000451184.1:n.*478G>A | |
| ENST00000553806.5:n.522G>A (SYNE2) | ||
| ENST00000554584.5:c.18480G>A (SYNE2) | ENSP00000452570.1:p.Arg6160= | |
| ENST00000554805.5:c.-49G>A (SYNE2) | ENSP00000450605.1:n.-49G>A | |
| ENST00000554997.1:n.397G>A (SYNE2) | ||
| ENST00000555002.5:c.8505G>A (SYNE2) | ENSP00000450831.1:p.Arg2835= | |
| ENST00000555022.5:c.237G>A (SYNE2) | ENSP00000451009.1:p.Arg79= | |
| ENST00000555612.5:c.*382G>A (SYNE2) | ENSP00000451972.1:n.*382G>A | |
| ENST00000556275.5:c.1406+24966C>T (ESR2) | ENSP00000452485.2:n.1406+24966C>T | |
| NM_015180.4:c.18603G>A (SYNE2) | NP_055995.4:p.Arg6201= | |
| NM_182914.2:c.18603G>A (SYNE2) | NP_878918.2:p.Arg6201= | |
| XM_005267454.1:c.18603G>A (SYNE2) | XP_005267511.1:p.Arg6201= | |
| XM_005267456.1:c.18603G>A (SYNE2) | XP_005267513.1:p.Arg6201= | |
| XM_005267457.1:c.18603G>A (SYNE2) | XP_005267514.1:p.Arg6201= | |
| XM_005267458.1:c.18603G>A (SYNE2) | XP_005267515.1:p.Arg6201= | |
| XM_005267459.1:c.18603G>A (SYNE2) | XP_005267516.1:p.Arg6201= | |
| XM_011536545.1:c.1406+24966C>T (ESR2) | XP_011534847.1:n.1406+24966C>T | |
| XM_011536574.1:c.18603G>A (SYNE2) | XP_011534876.1:p.Arg6201= | |
| XM_011536575.1:c.18603G>A (SYNE2) | XP_011534877.1:p.Arg6201= | |
| XM_011536576.1:c.18603G>A (SYNE2) | XP_011534878.1:p.Arg6201= | |
| XM_011536577.1:c.18603G>A (SYNE2) | XP_011534879.1:p.Arg6201= | |
| XM_011536578.1:c.18603G>A (SYNE2) | XP_011534880.1:p.Arg6201= | |
| XM_011536579.1:c.18603G>A (SYNE2) | XP_011534881.1:p.Arg6201= | |
| XM_011536580.1:c.18603G>A (SYNE2) | XP_011534882.1:p.Arg6201= | |
| XM_011536581.1:c.18603G>A (SYNE2) | XP_011534883.1:p.Arg6201= | |
| XM_011536582.1:c.18486G>A (SYNE2) | XP_011534884.1:p.Arg6162= | |
| XM_011536583.1:c.15408G>A (SYNE2) | XP_011534885.1:p.Arg5136= | |
| XM_011536575.2:c.18603G>A (SYNE2) | XP_011534877.1:p.Arg6201= | |
| XM_011536576.2:c.18603G>A (SYNE2) | XP_011534878.1:p.Arg6201= | |
| XM_011536577.2:c.18603G>A (SYNE2) | XP_011534879.1:p.Arg6201= | |
| XM_011536580.2:c.18603G>A (SYNE2) | XP_011534882.1:p.Arg6201= | |
| XM_017021101.1:c.18603G>A (SYNE2) | XP_016876590.1:p.Arg6201= | |
| XM_017021102.1:c.18534G>A (SYNE2) | XP_016876591.1:p.Arg6178= | |
| XM_017021103.2:c.585G>A (SYNE2) | XP_016876592.1:p.Arg195= | |
| XM_017021104.2:c.585G>A (SYNE2) | XP_016876593.1:p.Arg195= | |
| NM_015180.5:c.18603G>A (SYNE2) | NP_055995.4:p.Arg6201= | |
| NM_015180.6:c.18603G>A (SYNE2) | NP_055995.4:p.Arg6201= | |
| NM_182914.3:c.18603G>A (SYNE2) MANE Select | NP_878918.2:p.Arg6201= |