HGVS | Genome Assembly |
---|---|
NC_000023.11:g.8732012_8732014delinsCCG , CM000685.2:g.8732012_8732014delinsCCG | GRCh38 |
NC_000023.10:g.8700053_8700055delinsCCG , CM000685.1:g.8700053_8700055delinsCCG | GRCh37 |
NC_000023.9:g.8660053_8660055delinsCCG | NCBI36 |
NG_007088.1:g.5173_5175delinsCGG | |
NG_007088.2:g.5173_5175delinsCGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262648.8:c.23_25delinsCGG MANE Select | ENSP00000262648.3:p.Ala8= | |
ENST00000262648.7:c.23_25delinsCGG | ENSP00000262648.3:p.Ala8= | |
ENST00000619786.1:c.23_25delinsCGG | ENSP00000478734.1:p.Ala8= | |
NM_000216.2:c.23_25delinsCGG | NP_000207.2:p.Ala8= | |
XM_005274501.3:c.23_25delinsCGG | XP_005274558.1:p.Ala8= | |
NM_000216.3:c.23_25delinsCGG | NP_000207.2:p.Ala8= | |
XM_005274501.4:c.23_25delinsCGG | XP_005274558.1:p.Ala8= | |
NM_000216.4:c.23_25delinsCGG MANE Select | NP_000207.2:p.Ala8= |