Canonical Allele Identifier: CA637153547

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1346498494
• gnomAD v2: 21-19653463-T-TTAAATGG
• MyVariant Identifiers: chr21:g.19653463_19653464insTAAATGG (hg19) ; chr21:g.18281146_18281147insTAAATGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281146_18281147insTAAATGG , CM000683.2:g.18281146_18281147insTAAATGG	GRCh38
NC_000021.8:g.19653463_19653464insTAAATGG , CM000683.1:g.19653463_19653464insTAAATGG	GRCh37
NC_000021.7:g.18575334_18575335insTAAATGG	NCBI36
NG_012207.1:g.127507_127508insCCATTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2561_2562insCCATTTA MANE Select	ENSP00000284885.3:p.Val855HisfsTer9
ENST00000284885.7:c.2561_2562insCCATTTA	ENSP00000284885.3:p.Val855HisfsTer9
NM_002772.2:c.2561_2562insCCATTTA	NP_002763.2:p.Val855HisfsTer9
XM_011529654.1:c.2696_2697insCCATTTA	XP_011527956.1:p.Val900HisfsTer9
XM_011529655.1:c.2696_2697insCCATTTA	XP_011527957.1:p.Val900HisfsTer9
XM_011529656.1:c.2696_2697insCCATTTA	XP_011527958.1:p.Val900HisfsTer9
XM_011529657.1:c.2651_2652insCCATTTA	XP_011527959.1:p.Val885HisfsTer9
XM_011529658.1:c.2615_2616insCCATTTA	XP_011527960.1:p.Val873HisfsTer9
XM_011529659.1:c.2606_2607insCCATTTA	XP_011527961.1:p.Val870HisfsTer9
XM_011529654.2:c.2696_2697insCCATTTA	XP_011527956.1:p.Val900HisfsTer9
XM_011529656.2:c.2696_2697insCCATTTA	XP_011527958.1:p.Val900HisfsTer9
XM_011529657.2:c.2651_2652insCCATTTA	XP_011527959.1:p.Val885HisfsTer9
XM_011529658.2:c.2615_2616insCCATTTA	XP_011527960.1:p.Val873HisfsTer9
NM_002772.3:c.2561_2562insCCATTTA MANE Select	NP_002763.3:p.Val855HisfsTer9