Canonical Allele Identifier: CA552162420

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1470585341
• gnomAD v2: 4-68797706-C-T
• gnomAD v4: 4-67931988-C-T
• MyVariant Identifiers: chr4:g.68797706C>T (hg19) ; chr4:g.67931988C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67931988C>T , CM000666.2:g.67931988C>T	GRCh38
NC_000004.11:g.68797706C>T , CM000666.1:g.68797706C>T	GRCh37
NC_000004.10:g.68480301C>T	NCBI36

Transcript Alleles

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