Canonical Allele Identifier: CA2670825771

Gene: TMPRSS11A

Linked Data

• gnomAD v4: 4-67932155-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932155C>T , CM000666.2:g.67932155C>T	GRCh38
NC_000004.11:g.68797873C>T , CM000666.1:g.68797873C>T	GRCh37
NC_000004.10:g.68480468C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.253-95G>A MANE Select	ENSP00000426911.2:n.253-95G>A
ENST00000334830.11:c.262-95G>A	ENSP00000334611.7:n.262-95G>A
ENST00000396188.3:c.253-95G>A	ENSP00000379491.3:n.253-95G>A
ENST00000508048.5:c.253-95G>A	ENSP00000426911.2:n.253-95G>A
ENST00000513536.5:c.193-95G>A	ENSP00000427621.1:n.193-95G>A
NM_001114387.1:c.253-95G>A	NP_001107859.1:n.253-95G>A
NM_182606.3:c.262-95G>A	NP_872412.3:n.262-95G>A
NM_001114387.2:c.253-95G>A MANE Select	NP_001107859.1:n.253-95G>A
NM_182606.4:c.262-95G>A	NP_872412.3:n.262-95G>A