HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724924_174724925delinsTA , CM000667.2:g.174724924_174724925delinsTA | GRCh38 |
NC_000005.9:g.174151927_174151928delinsTA , CM000667.1:g.174151927_174151928delinsTA | GRCh37 |
NC_000005.8:g.174084533_174084534delinsTA | NCBI36 |
NG_008124.1:g.5353_5354delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.7:c.265_266delinsTA MANE Select | ENSP00000239243.5:p.Ala89Ter | |
ENST00000239243.6:c.265_266delinsTA | ENSP00000239243.5:p.Ala89Ter | |
ENST00000507785.2:c.265_266delinsTA | ENSP00000427425.1:p.Ala89Ter | |
NM_002449.4:c.265_266delinsTA | NP_002440.2:p.Ala89Ter | |
NM_001363626.1:c.265_266delinsTA | NP_001350555.1:p.Ala89Ter | |
NM_002449.5:c.265_266delinsTA MANE Select | NP_002440.2:p.Ala89Ter | |
NM_001363626.2:c.265_266delinsTA | NP_001350555.1:p.Ala89Ter |