Linked Data
ClinVar Variation Id:
1579034
ClinVar RCV Id:
RCV002102381
dbSNP Id:
rs2153506121
MyVariant Identifiers:
chr5:g.58511605A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.59215779A>G , CM000667.2:g.59215779A>G | GRCh38 |
| NC_000005.9:g.58511605A>G , CM000667.1:g.58511605A>G | GRCh37 |
| NC_000005.8:g.58547362A>G | NCBI36 |
| NG_027957.1:g.1277321T>C | |
| NG_027957.2:g.1313551T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507116.6:c.453T>C | ENSP00000424852.1:p.Asp151= | |
| ENST00000340635.11:c.645T>C MANE Select | ENSP00000345502.6:p.Asp215= | |
| ENST00000636120.1:c.315T>C | ENSP00000490821.1:p.Asp105= | |
| ENST00000638939.1:c.210T>C | ENSP00000492052.1:p.Asp70= | |
| ENST00000309641.10:c.453T>C | ENSP00000308485.6:p.Asp151= | |
| ENST00000340635.10:c.645T>C | ENSP00000345502.6:p.Asp215= | |
| ENST00000360047.9:c.237T>C | ENSP00000353152.5:p.Asp79= | |
| ENST00000405053.7:n.308T>C | ||
| ENST00000405755.6:c.279T>C | ENSP00000384806.2:p.Asp93= | |
| ENST00000502484.6:c.462T>C | ENSP00000423094.2:p.Asp154= | |
| ENST00000502575.1:c.453T>C | ENSP00000425917.1:p.Asp151= | |
| ENST00000503258.5:c.255T>C | ENSP00000425605.1:p.Asp85= | |
| ENST00000505453.1:c.-98-176808T>C | ENSP00000421013.1:n.-98-176808T>C | |
| ENST00000507116.5:c.453T>C | ENSP00000424852.1:p.Asp151= | |
| ENST00000514231.1:n.408T>C | ||
| ENST00000515324.1:n.157T>C | ||
| ENST00000546160.5:c.252T>C | ENSP00000442734.2:p.Asp84= | |
| ENST00000621323.4:n.190T>C | ||
| NM_001104631.1:c.645T>C | NP_001098101.1:p.Asp215= | |
| NM_001165899.1:c.462T>C | NP_001159371.1:p.Asp154= | |
| NM_001197218.1:c.453T>C | NP_001184147.1:p.Asp151= | |
| NM_001197219.1:c.279T>C | NP_001184148.1:p.Asp93= | |
| NM_001197220.1:c.255T>C | NP_001184149.1:p.Asp85= | |
| NM_006203.4:c.237T>C | NP_006194.2:p.Asp79= | |
| XM_005248537.2:c.315T>C | XP_005248594.1:p.Asp105= | |
| XM_005248538.3:c.237T>C | XP_005248595.1:p.Asp79= | |
| XM_011543469.1:c.609T>C | XP_011541771.1:p.Asp203= | |
| XM_011543470.1:c.609T>C | XP_011541772.1:p.Asp203= | |
| XM_011543471.1:c.462T>C | XP_011541773.1:p.Asp154= | |
| XM_011543472.1:c.462T>C | XP_011541774.1:p.Asp154= | |
| XM_011543473.1:c.462T>C | XP_011541775.1:p.Asp154= | |
| XM_011543474.1:c.432T>C | XP_011541776.1:p.Asp144= | |
| XM_011543475.1:c.279T>C | XP_011541777.1:p.Asp93= | |
| XM_011543476.1:c.225T>C | XP_011541778.1:p.Asp75= | |
| XM_011543477.1:c.204T>C | XP_011541779.1:p.Asp68= | |
| XM_011543478.1:c.141T>C | XP_011541780.1:p.Asp47= | |
| XM_011543479.1:c.141T>C | XP_011541781.1:p.Asp47= | |
| NM_001349241.1:c.432T>C | NP_001336170.1:p.Asp144= | |
| NM_001349242.1:c.315T>C | NP_001336171.1:p.Asp105= | |
| NM_001349243.1:c.-50T>C | NP_001336172.1:n.-50T>C | |
| NM_001364599.1:c.462T>C | NP_001351528.1:p.Asp154= | |
| NM_001364600.1:c.462T>C | NP_001351529.1:p.Asp154= | |
| NM_001364601.1:c.453T>C | NP_001351530.1:p.Asp151= | |
| NM_001364602.1:c.453T>C | NP_001351531.1:p.Asp151= | |
| NM_001364603.1:c.-306T>C | NP_001351532.1:n.-306T>C | |
| NM_001364604.1:c.-50T>C | NP_001351533.1:n.-50T>C | |
| XM_011543470.2:c.609T>C | XP_011541772.1:p.Asp203= | |
| XM_011543471.2:c.462T>C | XP_011541773.1:p.Asp154= | |
| XM_017009565.1:c.609T>C | XP_016865054.1:p.Asp203= | |
| XM_017009566.1:c.462T>C | XP_016865055.1:p.Asp154= | |
| XM_017009567.1:c.447T>C | XP_016865056.1:p.Asp149= | |
| XM_024446110.1:c.609T>C | XP_024301878.1:p.Asp203= | |
| XM_024446112.1:c.462T>C | XP_024301880.1:p.Asp154= | |
| NM_001104631.2:c.645T>C MANE Select | NP_001098101.1:p.Asp215= | |
| NM_001165899.2:c.462T>C | NP_001159371.1:p.Asp154= | |
| NM_001197218.2:c.453T>C | NP_001184147.1:p.Asp151= | |
| NM_001197219.2:c.279T>C | NP_001184148.1:p.Asp93= | |
| NM_001197220.2:c.255T>C | NP_001184149.1:p.Asp85= | |
| NM_001349241.2:c.432T>C | NP_001336170.1:p.Asp144= | |
| NM_001349243.2:c.-50T>C | NP_001336172.1:n.-50T>C | |
| NM_001364600.2:c.462T>C | NP_001351529.1:p.Asp154= | |
| NM_001364602.2:c.453T>C | NP_001351531.1:p.Asp151= | |
| NM_001349242.2:c.315T>C | NP_001336171.1:p.Asp105= | |
| NM_006203.5:c.237T>C | NP_006194.2:p.Asp79= |