Canonical Allele Identifier: CA2670825688

Gene: TMPRSS11A

Linked Data

• gnomAD v4: 4-67931973-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67931976del , CM000666.2:g.67931976del	GRCh38
NC_000004.11:g.68797694del , CM000666.1:g.68797694del	GRCh37
NC_000004.10:g.68480289del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.320+19del MANE Select	ENSP00000426911.2:n.320+19del
ENST00000334830.11:c.329+19del	ENSP00000334611.7:n.329+19del
ENST00000396188.3:c.320+19del	ENSP00000379491.3:n.320+19del
ENST00000508048.5:c.320+19del	ENSP00000426911.2:n.320+19del
ENST00000513536.5:c.260+19del	ENSP00000427621.1:n.260+19del
NM_001114387.1:c.320+19del	NP_001107859.1:n.320+19del
NM_182606.3:c.329+19del	NP_872412.3:n.329+19del
NM_001114387.2:c.320+19del MANE Select	NP_001107859.1:n.320+19del
NM_182606.4:c.329+19del	NP_872412.3:n.329+19del