Canonical Allele Identifier: CA98676712

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs745890637
• gnomAD v2: 4-68797726-T-G
• gnomAD v3: 4-67932008-T-G
• gnomAD v4: 4-67932008-T-G
• MyVariant Identifiers: chr4:g.68797726T>G (hg19) ; chr4:g.67932008T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932008T>G , CM000666.2:g.67932008T>G	GRCh38
NC_000004.11:g.68797726T>G , CM000666.1:g.68797726T>G	GRCh37
NC_000004.10:g.68480321T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.305A>C MANE Select	ENSP00000426911.2:p.Gln102Pro
ENST00000334830.11:c.314A>C	ENSP00000334611.7:p.Gln105Pro
ENST00000396188.3:c.305A>C	ENSP00000379491.3:p.Gln102Pro
ENST00000508048.5:c.305A>C	ENSP00000426911.2:p.Gln102Pro
ENST00000513536.5:c.245A>C	ENSP00000427621.1:p.Gln82Pro
NM_001114387.1:c.305A>C	NP_001107859.1:p.Gln102Pro
NM_182606.3:c.314A>C	NP_872412.3:p.Gln105Pro
NM_001114387.2:c.305A>C MANE Select	NP_001107859.1:p.Gln102Pro
NM_182606.4:c.314A>C	NP_872412.3:p.Gln105Pro