Canonical Allele Identifier: CA637153533

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1186013968
• gnomAD v2: 21-19653387-TC-T
• gnomAD v4: 21-18281070-TC-T
• MyVariant Identifiers: chr21:g.19653388del (hg19) ; chr21:g.18281071del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281071del , CM000683.2:g.18281071del	GRCh38
NC_000021.8:g.19653388del , CM000683.1:g.19653388del	GRCh37
NC_000021.7:g.18575259del	NCBI36
NG_012207.1:g.127583del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2637del MANE Select	ENSP00000284885.3:p.Met879IlefsTer8
ENST00000284885.7:c.2637del	ENSP00000284885.3:p.Met879IlefsTer8
NM_002772.2:c.2637del	NP_002763.2:p.Met879IlefsTer8
XM_011529654.1:c.2772del	XP_011527956.1:p.Met924IlefsTer8
XM_011529655.1:c.2772del	XP_011527957.1:p.Met924IlefsTer8
XM_011529656.1:c.2772del	XP_011527958.1:p.Met924IlefsTer8
XM_011529657.1:c.2727del	XP_011527959.1:p.Met909IlefsTer8
XM_011529658.1:c.2691del	XP_011527960.1:p.Met897IlefsTer8
XM_011529659.1:c.2682del	XP_011527961.1:p.Met894IlefsTer8
XM_011529654.2:c.2772del	XP_011527956.1:p.Met924IlefsTer8
XM_011529656.2:c.2772del	XP_011527958.1:p.Met924IlefsTer8
XM_011529657.2:c.2727del	XP_011527959.1:p.Met909IlefsTer8
XM_011529658.2:c.2691del	XP_011527960.1:p.Met897IlefsTer8
NM_002772.3:c.2637del MANE Select	NP_002763.3:p.Met879IlefsTer8