Linked Data
dbSNP Id:
rs886576286
gnomAD v2:
15-38647809-A-AATC
gnomAD v3:
15-38355608-A-AATC
gnomAD v4:
15-38355608-A-AATC
MyVariant Identifiers:
chr15:g.38647809_38647810insATC (hg19)
chr15:g.38355608_38355609insATC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38355609_38355610insTCA , CM000677.2:g.38355609_38355610insTCA | GRCh38 |
| NC_000015.9:g.38647810_38647811insTCA , CM000677.1:g.38647810_38647811insTCA | GRCh37 |
| NC_000015.8:g.36435102_36435103insTCA | NCBI36 |
| NG_008980.1:g.107759_107760insTCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.*3945_*3946insTCA MANE Select | ENSP00000299084.4:n.*3945_*3946insTCA | |
| ENST00000299084.8:c.*3945_*3946insTCA | ENSP00000299084.4:n.*3945_*3946insTCA | |
| NM_152594.2:c.*3945_*3946insTCA | NP_689807.1:n.*3945_*3946insTCA | |
| XM_005254202.2:c.*3945_*3946insTCA | XP_005254259.1:n.*3945_*3946insTCA | |
| XM_005254203.3:c.*3945_*3946insTCA | XP_005254260.1:n.*3945_*3946insTCA | |
| XM_011521288.1:c.*3945_*3946insTCA | XP_011519590.1:n.*3945_*3946insTCA | |
| XM_011521289.1:c.*3945_*3946insTCA | XP_011519591.1:n.*3945_*3946insTCA | |
| XM_011521290.1:c.*3945_*3946insTCA | XP_011519592.1:n.*3945_*3946insTCA | |
| XM_005254202.3:c.*3945_*3946insTCA | XP_005254259.1:n.*3945_*3946insTCA | |
| XM_011521289.3:c.*3945_*3946insTCA | XP_011519591.1:n.*3945_*3946insTCA | |
| NM_152594.3:c.*3945_*3946insTCA MANE Select | NP_689807.1:n.*3945_*3946insTCA |