HGVS | Genome Assembly |
---|---|
NC_000008.11:g.115414018A= , CM000670.2:g.115414018A= | GRCh38 |
NC_000008.10:g.116426246A= , CM000670.1:g.116426246A= | GRCh37 |
NC_000008.9:g.116495422A= | NCBI36 |
NG_012383.3:g.259984T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395715.8:c.*5T= MANE Select | ENSP00000379065.3:n.*5T= | |
ENST00000640765.1:c.*5T= | ENSP00000492037.1:n.*5T= | |
ENST00000220888.9:c.*5T= | ENSP00000220888.5:n.*5T= | |
ENST00000395715.7:c.*5T= | ENSP00000379065.3:n.*5T= | |
ENST00000519076.5:c.*5T= | ENSP00000428910.1:n.*5T= | |
ENST00000520276.5:c.*5T= | ENSP00000428680.1:n.*5T= | |
NM_001282902.2:c.*5T= | NP_001269831.1:n.*5T= | |
NM_001282903.2:c.*5T= | NP_001269832.1:n.*5T= | |
NM_014112.4:c.*5T= | NP_054831.2:n.*5T= | |
XM_005251049.2:c.*5T= | XP_005251106.1:n.*5T= | |
XM_006716625.1:c.*5T= | XP_006716688.1:n.*5T= | |
XM_011517264.1:c.*5T= | XP_011515566.1:n.*5T= | |
XM_011517265.1:c.*5T= | XP_011515567.1:n.*5T= | |
XM_011517266.1:c.*5T= | XP_011515568.1:n.*5T= | |
XM_011517267.1:c.*5T= | XP_011515569.1:n.*5T= | |
XM_011517268.1:c.*5T= | XP_011515570.1:n.*5T= | |
NM_001330599.1:c.*5T= | NP_001317528.1:n.*5T= | |
XM_011517264.2:c.*5T= | XP_011515566.1:n.*5T= | |
XM_011517266.3:c.*5T= | XP_011515568.1:n.*5T= | |
XM_011517268.2:c.*5T= | XP_011515570.1:n.*5T= | |
NM_001282902.3:c.*5T= | NP_001269831.1:n.*5T= | |
NM_001282903.3:c.*5T= | NP_001269832.1:n.*5T= | |
NM_001330599.2:c.*5T= | NP_001317528.1:n.*5T= | |
NM_014112.5:c.*5T= MANE Select | NP_054831.2:n.*5T= |