Canonical Allele Identifier: CA797724096

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1385654425
• gnomAD v3: 4-67932143-C-A
• gnomAD v4: 4-67932143-C-A
• MyVariant Identifiers: chr4:g.68797861C>A (hg19) ; chr4:g.67932143C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932143C>A , CM000666.2:g.67932143C>A	GRCh38
NC_000004.11:g.68797861C>A , CM000666.1:g.68797861C>A	GRCh37
NC_000004.10:g.68480456C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.253-83G>T MANE Select	ENSP00000426911.2:n.253-83G>T
ENST00000334830.11:c.262-83G>T	ENSP00000334611.7:n.262-83G>T
ENST00000396188.3:c.253-83G>T	ENSP00000379491.3:n.253-83G>T
ENST00000508048.5:c.253-83G>T	ENSP00000426911.2:n.253-83G>T
ENST00000513536.5:c.193-83G>T	ENSP00000427621.1:n.193-83G>T
NM_001114387.1:c.253-83G>T	NP_001107859.1:n.253-83G>T
NM_182606.3:c.262-83G>T	NP_872412.3:n.262-83G>T
NM_001114387.2:c.253-83G>T MANE Select	NP_001107859.1:n.253-83G>T
NM_182606.4:c.262-83G>T	NP_872412.3:n.262-83G>T