Canonical Allele Identifier: CA511459090

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653364A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281047A>G , CM000683.2:g.18281047A>G	GRCh38
NC_000021.8:g.19653364A>G , CM000683.1:g.19653364A>G	GRCh37
NC_000021.7:g.18575235A>G	NCBI36
NG_012207.1:g.127607T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2661T>C MANE Select	ENSP00000284885.3:p.Asn887=
ENST00000284885.7:c.2661T>C	ENSP00000284885.3:p.Asn887=
NM_002772.2:c.2661T>C	NP_002763.2:p.Asn887=
XM_011529654.1:c.2796T>C	XP_011527956.1:p.Asn932=
XM_011529655.1:c.2796T>C	XP_011527957.1:p.Asn932=
XM_011529656.1:c.2796T>C	XP_011527958.1:p.Asn932=
XM_011529657.1:c.2751T>C	XP_011527959.1:p.Asn917=
XM_011529658.1:c.2715T>C	XP_011527960.1:p.Asn905=
XM_011529659.1:c.2706T>C	XP_011527961.1:p.Asn902=
XM_011529654.2:c.2796T>C	XP_011527956.1:p.Asn932=
XM_011529656.2:c.2796T>C	XP_011527958.1:p.Asn932=
XM_011529657.2:c.2751T>C	XP_011527959.1:p.Asn917=
XM_011529658.2:c.2715T>C	XP_011527960.1:p.Asn905=
NM_002772.3:c.2661T>C MANE Select	NP_002763.3:p.Asn887=