Canonical Allele Identifier: CA552162421

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1157949658
• gnomAD v2: 4-68797707-A-G
• gnomAD v4: 4-67931989-A-G
• MyVariant Identifiers: chr4:g.68797707A>G (hg19) ; chr4:g.67931989A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67931989A>G , CM000666.2:g.67931989A>G	GRCh38
NC_000004.11:g.68797707A>G , CM000666.1:g.68797707A>G	GRCh37
NC_000004.10:g.68480302A>G	NCBI36

Transcript Alleles

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