Canonical Allele Identifier: CA357064402

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1393926730
• gnomAD v2: 4-68797724-C-T
• gnomAD v3: 4-67932006-C-T
• gnomAD v4: 4-67932006-C-T
• MyVariant Identifiers: chr4:g.68797724C>T (hg19) ; chr4:g.67932006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932006C>T , CM000666.2:g.67932006C>T	GRCh38
NC_000004.11:g.68797724C>T , CM000666.1:g.68797724C>T	GRCh37
NC_000004.10:g.68480319C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.307G>A MANE Select	ENSP00000426911.2:p.Val103Ile
ENST00000334830.11:c.316G>A	ENSP00000334611.7:p.Val106Ile
ENST00000396188.3:c.307G>A	ENSP00000379491.3:p.Val103Ile
ENST00000508048.5:c.307G>A	ENSP00000426911.2:p.Val103Ile
ENST00000513536.5:c.247G>A	ENSP00000427621.1:p.Val83Ile
NM_001114387.1:c.307G>A	NP_001107859.1:p.Val103Ile
NM_182606.3:c.316G>A	NP_872412.3:p.Val106Ile
NM_001114387.2:c.307G>A MANE Select	NP_001107859.1:p.Val103Ile
NM_182606.4:c.316G>A	NP_872412.3:p.Val106Ile