Canonical Allele Identifier: CA9983977
Gene: TMPRSS15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1970982
ClinVar RCV Id: RCV002760543
dbSNP Id: rs3215891
ExAC: 21:19653342 A / AT
gnomAD v2: 21-19653342-A-AT
gnomAD v3: 21-18281025-A-AT
gnomAD v4: 21-18281025-A-AT
MyVariant Identifiers: chr21:g.19653346_19653347insT (hg19) chr21:g.19653345_19653346insT (hg19) chr21:g.19653344_19653345insT (hg19) chr21:g.19653342_19653343insT (hg19) chr21:g.18281028_18281029insT (hg38) chr21:g.18281025_18281026insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281037dup , CM000683.2:g.18281037dup GRCh38
NC_000021.8:g.19653354dup , CM000683.1:g.19653354dup GRCh37
NC_000021.7:g.18575225dup NCBI36
NG_012207.1:g.127628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2668+14dup MANE Select ENSP00000284885.3:n.2668+14dup
ENST00000284885.7:c.2668+14dup ENSP00000284885.3:n.2668+14dup
NM_002772.2:c.2668+14dup NP_002763.2:n.2668+14dup
XM_011529654.1:c.2803+14dup XP_011527956.1:n.2803+14dup
XM_011529655.1:c.2803+14dup XP_011527957.1:n.2803+14dup
XM_011529656.1:c.2803+14dup XP_011527958.1:n.2803+14dup
XM_011529657.1:c.2758+14dup XP_011527959.1:n.2758+14dup
XM_011529658.1:c.2722+14dup XP_011527960.1:n.2722+14dup
XM_011529659.1:c.2713+14dup XP_011527961.1:n.2713+14dup
XM_011529654.2:c.2803+14dup XP_011527956.1:n.2803+14dup
XM_011529656.2:c.2803+14dup XP_011527958.1:n.2803+14dup
XM_011529657.2:c.2758+14dup XP_011527959.1:n.2758+14dup
XM_011529658.2:c.2722+14dup XP_011527960.1:n.2722+14dup
NM_002772.3:c.2668+14dup MANE Select NP_002763.3:n.2668+14dup
Search 100 bp 5'
Search 100 bp 3'