Canonical Allele Identifier: CA409847998

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1190348912
• gnomAD v4: 21-18281115-T-G
• COSMIC: COSM4100872
• MyVariant Identifiers: chr21:g.19653432T>G (hg19) ; chr21:g.18281115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281115T>G , CM000683.2:g.18281115T>G	GRCh38
NC_000021.8:g.19653432T>G , CM000683.1:g.19653432T>G	GRCh37
NC_000021.7:g.18575303T>G	NCBI36
NG_012207.1:g.127539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2593A>C MANE Select	ENSP00000284885.3:p.Asn865His
ENST00000284885.7:c.2593A>C	ENSP00000284885.3:p.Asn865His
NM_002772.2:c.2593A>C	NP_002763.2:p.Asn865His
XM_011529654.1:c.2728A>C	XP_011527956.1:p.Asn910His
XM_011529655.1:c.2728A>C	XP_011527957.1:p.Asn910His
XM_011529656.1:c.2728A>C	XP_011527958.1:p.Asn910His
XM_011529657.1:c.2683A>C	XP_011527959.1:p.Asn895His
XM_011529658.1:c.2647A>C	XP_011527960.1:p.Asn883His
XM_011529659.1:c.2638A>C	XP_011527961.1:p.Asn880His
XM_011529654.2:c.2728A>C	XP_011527956.1:p.Asn910His
XM_011529656.2:c.2728A>C	XP_011527958.1:p.Asn910His
XM_011529657.2:c.2683A>C	XP_011527959.1:p.Asn895His
XM_011529658.2:c.2647A>C	XP_011527960.1:p.Asn883His
NM_002772.3:c.2593A>C MANE Select	NP_002763.3:p.Asn865His