Canonical Allele Identifier: CA9984008
Gene: TMPRSS15 HGNC NCBI

Linked Data

ClinVar Variation Id: 782931
dbSNP Id: rs200483285

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281172T>G , CM000683.2:g.18281172T>G GRCh38
NC_000021.8:g.19653489T>G , CM000683.1:g.19653489T>G GRCh37
NC_000021.7:g.18575360T>G NCBI36
NG_012207.1:g.127482A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2536A>C MANE Select ENSP00000284885.3:p.Lys846Gln
ENST00000284885.7:c.2536A>C ENSP00000284885.3:p.Lys846Gln
NM_002772.2:c.2536A>C NP_002763.2:p.Lys846Gln
XM_011529654.1:c.2671A>C XP_011527956.1:p.Lys891Gln
XM_011529655.1:c.2671A>C XP_011527957.1:p.Lys891Gln
XM_011529656.1:c.2671A>C XP_011527958.1:p.Lys891Gln
XM_011529657.1:c.2626A>C XP_011527959.1:p.Lys876Gln
XM_011529658.1:c.2590A>C XP_011527960.1:p.Lys864Gln
XM_011529659.1:c.2581A>C XP_011527961.1:p.Lys861Gln
XM_011529654.2:c.2671A>C XP_011527956.1:p.Lys891Gln
XM_011529656.2:c.2671A>C XP_011527958.1:p.Lys891Gln
XM_011529657.2:c.2626A>C XP_011527959.1:p.Lys876Gln
XM_011529658.2:c.2590A>C XP_011527960.1:p.Lys864Gln
NM_002772.3:c.2536A>C MANE Select NP_002763.3:p.Lys846Gln