Canonical Allele Identifier: CA637153532

Gene: TMPRSS15

Linked Data

• gnomAD v2: 21-19653357-C-CTT
• gnomAD v3: 21-18281040-C-CTT
• gnomAD v4: 21-18281040-C-CTT
• MyVariant Identifiers: chr21:g.19653359_19653361delinsTTGTG (hg19) ; chr21:g.19653357_19653358insTT (hg19) ; chr21:g.18281040_18281041insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281041_18281042insTT , CM000683.2:g.18281041_18281042insTT	GRCh38
NC_000021.8:g.19653358_19653359insTT , CM000683.1:g.19653358_19653359insTT	GRCh37
NC_000021.7:g.18575229_18575230insTT	NCBI36
NG_012207.1:g.127613_127614insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2667_2668insAA MANE Select	ENSP00000284885.3:p.Asp890LysfsTer?
ENST00000284885.7:c.2667_2668insAA	ENSP00000284885.3:p.Asp890LysfsTer?
NM_002772.2:c.2667_2668insAA	NP_002763.2:p.Asp890LysfsTer?
XM_011529654.1:c.2802_2803insAA	XP_011527956.1:p.Asp935LysfsTer?
XM_011529655.1:c.2802_2803insAA	XP_011527957.1:p.Asp935LysfsTer?
XM_011529656.1:c.2802_2803insAA	XP_011527958.1:p.Asp935LysfsTer?
XM_011529657.1:c.2757_2758insAA	XP_011527959.1:p.Asp920LysfsTer?
XM_011529658.1:c.2721_2722insAA	XP_011527960.1:p.Asp908LysfsTer?
XM_011529659.1:c.2712_2713insAA	XP_011527961.1:p.Asp905LysfsTer?
XM_011529654.2:c.2802_2803insAA	XP_011527956.1:p.Asp935LysfsTer?
XM_011529656.2:c.2802_2803insAA	XP_011527958.1:p.Asp935LysfsTer?
XM_011529657.2:c.2757_2758insAA	XP_011527959.1:p.Asp920LysfsTer?
XM_011529658.2:c.2721_2722insAA	XP_011527960.1:p.Asp908LysfsTer?
NM_002772.3:c.2667_2668insAA MANE Select	NP_002763.3:p.Asp890LysfsTer?