Canonical Allele Identifier: CA2379736665

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074692710
• gnomAD v4: 21-18281106-AATGAGGGTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281111_18281120del , CM000683.2:g.18281111_18281120del	GRCh38
NC_000021.8:g.19653428_19653437del , CM000683.1:g.19653428_19653437del	GRCh37
NC_000021.7:g.18575299_18575308del	NCBI36
NG_012207.1:g.127538_127547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2592_2601del MANE Select	ENSP00000284885.3:p.Asn865ThrfsTer12
ENST00000284885.7:c.2592_2601del	ENSP00000284885.3:p.Asn865ThrfsTer12
NM_002772.2:c.2592_2601del	NP_002763.2:p.Asn865ThrfsTer12
XM_011529654.1:c.2727_2736del	XP_011527956.1:p.Asn910ThrfsTer12
XM_011529655.1:c.2727_2736del	XP_011527957.1:p.Asn910ThrfsTer12
XM_011529656.1:c.2727_2736del	XP_011527958.1:p.Asn910ThrfsTer12
XM_011529657.1:c.2682_2691del	XP_011527959.1:p.Asn895ThrfsTer12
XM_011529658.1:c.2646_2655del	XP_011527960.1:p.Asn883ThrfsTer12
XM_011529659.1:c.2637_2646del	XP_011527961.1:p.Asn880ThrfsTer12
XM_011529654.2:c.2727_2736del	XP_011527956.1:p.Asn910ThrfsTer12
XM_011529656.2:c.2727_2736del	XP_011527958.1:p.Asn910ThrfsTer12
XM_011529657.2:c.2682_2691del	XP_011527959.1:p.Asn895ThrfsTer12
XM_011529658.2:c.2646_2655del	XP_011527960.1:p.Asn883ThrfsTer12
NM_002772.3:c.2592_2601del MANE Select	NP_002763.3:p.Asn865ThrfsTer12