HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38148683_38148684delinsTA , CM000670.2:g.38148683_38148684delinsTA | GRCh38 |
NC_000008.10:g.38006201_38006202delinsTA , CM000670.1:g.38006201_38006202delinsTA | GRCh37 |
NC_000008.9:g.38125358_38125359delinsTA | NCBI36 |
NG_011827.1:g.7399_7400delinsTA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.135_136delinsTA MANE Select | ENSP00000276449.3:p.Pro45= | |
ENST00000276449.8:c.135_136delinsTA | ENSP00000276449.3:p.Pro45= | |
ENST00000520114.1:n.309_310delinsTA | ||
ENST00000521236.1:c.-144_-143delinsTA | ENSP00000430030.1:n.-144_-143delinsTA | |
ENST00000522050.1:c.71_72delinsTA | ||
NM_000349.2:c.135_136delinsTA | NP_000340.2:p.Pro45= | |
XM_006716392.1:c.135_136delinsTA | XP_006716455.1:p.Pro45= | |
NM_000349.3:c.135_136delinsTA MANE Select | NP_000340.2:p.Pro45= |