Canonical Allele Identifier: CA552162433

Gene: TMPRSS11A

Linked Data

• gnomAD v2: 4-68797746-C-CATAAACATTACCT
• MyVariant Identifiers: chr4:g.68797747_68797761delinsATAAACATTACCTTTCCAGGCTGAATCT (hg19) ; chr4:g.67932029_67932043delinsATAAACATTACCTTTCCAGGCTGAATCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932028_67932029insATAAACATTACCT , CM000666.2:g.67932028_67932029insATAAACATTACCT	GRCh38
NC_000004.11:g.68797746_68797747insATAAACATTACCT , CM000666.1:g.68797746_68797747insATAAACATTACCT	GRCh37
NC_000004.10:g.68480341_68480342insATAAACATTACCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.284_285insAGGTAATGTTTAT MANE Select	ENSP00000426911.2:p.Lys96GlyfsTer?
ENST00000334830.11:c.293_294insAGGTAATGTTTAT	ENSP00000334611.7:p.Lys99GlyfsTer?
ENST00000396188.3:c.284_285insAGGTAATGTTTAT	ENSP00000379491.3:p.Lys96GlyfsTer?
ENST00000508048.5:c.284_285insAGGTAATGTTTAT	ENSP00000426911.2:p.Lys96GlyfsTer?
ENST00000513536.5:c.224_225insAGGTAATGTTTAT	ENSP00000427621.1:p.Lys76GlyfsTer?
NM_001114387.1:c.284_285insAGGTAATGTTTAT	NP_001107859.1:p.Lys96GlyfsTer?
NM_182606.3:c.293_294insAGGTAATGTTTAT	NP_872412.3:p.Lys99GlyfsTer?
NM_001114387.2:c.284_285insAGGTAATGTTTAT MANE Select	NP_001107859.1:p.Lys96GlyfsTer?
NM_182606.4:c.293_294insAGGTAATGTTTAT	NP_872412.3:p.Lys99GlyfsTer?