MyVariant.info:
GRCh37
chr4:g.5564740A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5563013A>G , CM000666.2:g.5563013A>G | GRCh38 |
| NC_000004.11:g.5564740A>G , CM000666.1:g.5564740A>G | GRCh37 |
| NC_000004.10:g.5615641A>G | NCBI36 |
| NG_015821.1:g.151536T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344408.10:c.3762T>C MANE Select | ENSP00000342144.5:p.Pro1254= | |
| ENST00000310917.6:c.3522T>C | ENSP00000311683.2:p.Pro1174= | |
| ENST00000344408.9:c.3762T>C | ENSP00000342144.5:p.Pro1254= | |
| ENST00000475313.5:c.3419+2245T>C | ENSP00000431981.1:n.3419+2245T>C | |
| ENST00000509670.1:c.*2155T>C | ENSP00000423876.1:n.*2155T>C | |
| NM_001166136.1:c.3522T>C | NP_001159608.1:p.Pro1174= | |
| NM_147127.4:c.3762T>C | NP_667338.3:p.Pro1254= | |
| XM_011513392.1:c.3771T>C | XP_011511694.1:p.Pro1257= | |
| XM_011513393.1:c.3668+2245T>C | XP_011511695.1:n.3668+2245T>C | |
| XM_011513394.1:c.3531T>C | XP_011511696.1:p.Pro1177= | |
| XM_017007736.1:c.3522T>C | XP_016863225.1:p.Pro1174= | |
| XM_017007737.1:c.3522T>C | XP_016863226.1:p.Pro1174= | |
| XM_017007739.1:c.2082T>C | XP_016863228.1:p.Pro694= | |
| XM_024453893.1:c.2082T>C | XP_024309661.1:p.Pro694= | |
| XR_001741141.1:n.3612T>C | ||
| NM_147127.5:c.3762T>C MANE Select | NP_667338.3:p.Pro1254= | |
| NM_001166136.2:c.3522T>C | NP_001159608.1:p.Pro1174= |