Canonical Allele Identifier: CA203863
Gene: TMPRSS15 HGNC NCBI

Linked Data

ClinVar Variation Id: 202209
dbSNP Id: rs138221037

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18343504A>C , CM000683.2:g.18343504A>C GRCh38
NC_000021.8:g.19715821A>C , CM000683.1:g.19715821A>C GRCh37
NC_000021.7:g.18637692A>C NCBI36
NG_012207.1:g.65150T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284885.8:c.1428+2T>G MANE Select ENSP00000284885.3:n.1428+2T>G
ENST00000284885.7:c.1428+2T>G ENSP00000284885.3:n.1428+2T>G
NM_002772.2:c.1428+2T>G NP_002763.2:n.1428+2T>G
XM_011529654.1:c.1563+2T>G XP_011527956.1:n.1563+2T>G
XM_011529655.1:c.1563+2T>G XP_011527957.1:n.1563+2T>G
XM_011529656.1:c.1563+2T>G XP_011527958.1:n.1563+2T>G
XM_011529657.1:c.1518+2T>G XP_011527959.1:n.1518+2T>G
XM_011529658.1:c.1482+2T>G XP_011527960.1:n.1482+2T>G
XM_011529659.1:c.1473+2T>G XP_011527961.1:n.1473+2T>G
XM_011529654.2:c.1563+2T>G XP_011527956.1:n.1563+2T>G
XM_011529656.2:c.1563+2T>G XP_011527958.1:n.1563+2T>G
XM_011529657.2:c.1518+2T>G XP_011527959.1:n.1518+2T>G
XM_011529658.2:c.1482+2T>G XP_011527960.1:n.1482+2T>G
NM_002772.3:c.1428+2T>G MANE Select NP_002763.3:n.1428+2T>G