Canonical Allele Identifier: CA409847951
Gene: TMPRSS15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281093C>G , CM000683.2:g.18281093C>G GRCh38
NC_000021.8:g.19653410C>G , CM000683.1:g.19653410C>G GRCh37
NC_000021.7:g.18575281C>G NCBI36
NG_012207.1:g.127561G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2615G>C MANE Select ENSP00000284885.3:p.Arg872Thr
ENST00000284885.7:c.2615G>C ENSP00000284885.3:p.Arg872Thr
NM_002772.2:c.2615G>C NP_002763.2:p.Arg872Thr
XM_011529654.1:c.2750G>C XP_011527956.1:p.Arg917Thr
XM_011529655.1:c.2750G>C XP_011527957.1:p.Arg917Thr
XM_011529656.1:c.2750G>C XP_011527958.1:p.Arg917Thr
XM_011529657.1:c.2705G>C XP_011527959.1:p.Arg902Thr
XM_011529658.1:c.2669G>C XP_011527960.1:p.Arg890Thr
XM_011529659.1:c.2660G>C XP_011527961.1:p.Arg887Thr
XM_011529654.2:c.2750G>C XP_011527956.1:p.Arg917Thr
XM_011529656.2:c.2750G>C XP_011527958.1:p.Arg917Thr
XM_011529657.2:c.2705G>C XP_011527959.1:p.Arg902Thr
XM_011529658.2:c.2669G>C XP_011527960.1:p.Arg890Thr
NM_002772.3:c.2615G>C MANE Select NP_002763.3:p.Arg872Thr