Linked Data
dbSNP Id:
rs1286023547
MyVariant Identifiers:
chr2:g.190925029_190925030insAC (hg19)
chr2:g.190060303_190060304insAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.190060303_190060304insAC , CM000664.2:g.190060303_190060304insAC | GRCh38 |
| NC_000002.11:g.190925029_190925030insAC , CM000664.1:g.190925029_190925030insAC | GRCh37 |
| NC_000002.10:g.190633274_190633275insAC | NCBI36 |
| NG_009800.1:g.7426_7427insGT , LRG_200:g.7426_7427insGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260950.5:c.505_506insGT (MSTN) MANE Select | ENSP00000260950.3:p.Val169GlyfsTer7 | |
| ENST00000260950.4:c.505_506insGT (MSTN) | ENSP00000260950.3:p.Val169GlyfsTer7 | |
| ENST00000478197.1:n.220-18920_220-18919insAC (C2orf88) | ||
| ENST00000495546.1:n.202-19651_202-19650insAC (C2orf88) | ||
| NM_005259.2:c.505_506insGT , LRG_200t1:c.505_506insGT (MSTN) | NP_005250.1:p.Val169GlyfsTer7 | |
| XM_005246905.1:c.-359-19651_-359-19650insAC (C2orf88) | XP_005246962.1:n.-359-19651_-359-19650insAC | |
| XM_011510958.1:c.121_122insGT (MSTN) | XP_011509260.1:p.Val41GlyfsTer7 | |
| XM_011511982.1:c.-433-19651_-433-19650insAC (C2orf88) | XP_011510284.1:n.-433-19651_-433-19650insAC | |
| XM_011511986.1:c.-234-19651_-234-19650insAC (C2orf88) | XP_011510288.1:n.-234-19651_-234-19650insAC | |
| XM_011511986.2:c.-234-19651_-234-19650insAC (C2orf88) | XP_011510288.1:n.-234-19651_-234-19650insAC | |
| NM_005259.3:c.505_506insGT (MSTN) MANE Select | NP_005250.1:p.Val169GlyfsTer7 |