HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547251_31547253dup , CM000680.2:g.31547251_31547253dup | GRCh38 |
NC_000018.9:g.29127214_29127216dup , CM000680.1:g.29127214_29127216dup | GRCh37 |
NC_000018.8:g.27381212_27381214dup | NCBI36 |
NG_007072.3:g.54010_54012dup , LRG_397:g.54010_54012dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*508_*510dup (DSG2) MANE Select | ENSP00000261590.8:n.*508_*510dup | |
ENST00000261590.12:c.*508_*510dup (DSG2) | ENSP00000261590.8:n.*508_*510dup | |
NM_001943.3:c.*508_*510dup , LRG_397t1:c.*508_*510dup (DSG2) | NP_001934.2:n.*508_*510dup | |
NR_045216.1:n.1346-1344_1346-1342dup (DSG2-AS1) | ||
NM_001943.4:c.*508_*510dup (DSG2) | NP_001934.2:n.*508_*510dup | |
XM_024451095.1:c.*508_*510dup (DSG2) | XP_024306863.1:n.*508_*510dup | |
NM_001943.5:c.*508_*510dup (DSG2) MANE Select | NP_001934.2:n.*508_*510dup |