Canonical Allele Identifier: CA9984003

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs144134985
• ExAC: 21:19653458 G / C
• gnomAD v2: 21-19653458-G-C
• gnomAD v3: 21-18281141-G-C
• gnomAD v4: 21-18281141-G-C
• MyVariant Identifiers: chr21:g.19653458G>C (hg19) ; chr21:g.18281141G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281141G>C , CM000683.2:g.18281141G>C	GRCh38
NC_000021.8:g.19653458G>C , CM000683.1:g.19653458G>C	GRCh37
NC_000021.7:g.18575329G>C	NCBI36
NG_012207.1:g.127513C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2567C>G MANE Select	ENSP00000284885.3:p.Pro856Arg
ENST00000284885.7:c.2567C>G	ENSP00000284885.3:p.Pro856Arg
NM_002772.2:c.2567C>G	NP_002763.2:p.Pro856Arg
XM_011529654.1:c.2702C>G	XP_011527956.1:p.Pro901Arg
XM_011529655.1:c.2702C>G	XP_011527957.1:p.Pro901Arg
XM_011529656.1:c.2702C>G	XP_011527958.1:p.Pro901Arg
XM_011529657.1:c.2657C>G	XP_011527959.1:p.Pro886Arg
XM_011529658.1:c.2621C>G	XP_011527960.1:p.Pro874Arg
XM_011529659.1:c.2612C>G	XP_011527961.1:p.Pro871Arg
XM_011529654.2:c.2702C>G	XP_011527956.1:p.Pro901Arg
XM_011529656.2:c.2702C>G	XP_011527958.1:p.Pro901Arg
XM_011529657.2:c.2657C>G	XP_011527959.1:p.Pro886Arg
XM_011529658.2:c.2621C>G	XP_011527960.1:p.Pro874Arg
NM_002772.3:c.2567C>G MANE Select	NP_002763.3:p.Pro856Arg