Canonical Allele Identifier: CA409847951

Gene: TMPRSS15

Linked Data

• COSMIC: COSM3423868
• MyVariant Identifiers: chr21:g.19653410C>G (hg19) ; chr21:g.18281093C>G (hg38)

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