Canonical Allele Identifier: CA409847965

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653418A>C (hg19) ; chr21:g.18281101A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281101A>C , CM000683.2:g.18281101A>C	GRCh38
NC_000021.8:g.19653418A>C , CM000683.1:g.19653418A>C	GRCh37
NC_000021.7:g.18575289A>C	NCBI36
NG_012207.1:g.127553T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2607T>G MANE Select	ENSP00000284885.3:p.Asn869Lys
ENST00000284885.7:c.2607T>G	ENSP00000284885.3:p.Asn869Lys
NM_002772.2:c.2607T>G	NP_002763.2:p.Asn869Lys
XM_011529654.1:c.2742T>G	XP_011527956.1:p.Asn914Lys
XM_011529655.1:c.2742T>G	XP_011527957.1:p.Asn914Lys
XM_011529656.1:c.2742T>G	XP_011527958.1:p.Asn914Lys
XM_011529657.1:c.2697T>G	XP_011527959.1:p.Asn899Lys
XM_011529658.1:c.2661T>G	XP_011527960.1:p.Asn887Lys
XM_011529659.1:c.2652T>G	XP_011527961.1:p.Asn884Lys
XM_011529654.2:c.2742T>G	XP_011527956.1:p.Asn914Lys
XM_011529656.2:c.2742T>G	XP_011527958.1:p.Asn914Lys
XM_011529657.2:c.2697T>G	XP_011527959.1:p.Asn899Lys
XM_011529658.2:c.2661T>G	XP_011527960.1:p.Asn887Lys
NM_002772.3:c.2607T>G MANE Select	NP_002763.3:p.Asn869Lys