Canonical Allele Identifier: CA552162410

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1285992522
• gnomAD v2: 4-68797678-C-G
• gnomAD v4: 4-67931960-C-G
• MyVariant Identifiers: chr4:g.68797678C>G (hg19) ; chr4:g.67931960C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67931960C>G , CM000666.2:g.67931960C>G	GRCh38
NC_000004.11:g.68797678C>G , CM000666.1:g.68797678C>G	GRCh37
NC_000004.10:g.68480273C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.320+33G>C MANE Select	ENSP00000426911.2:n.320+33G>C
ENST00000334830.11:c.329+33G>C	ENSP00000334611.7:n.329+33G>C
ENST00000396188.3:c.320+33G>C	ENSP00000379491.3:n.320+33G>C
ENST00000508048.5:c.320+33G>C	ENSP00000426911.2:n.320+33G>C
ENST00000513536.5:c.260+33G>C	ENSP00000427621.1:n.260+33G>C
NM_001114387.1:c.320+33G>C	NP_001107859.1:n.320+33G>C
NM_182606.3:c.329+33G>C	NP_872412.3:n.329+33G>C
NM_001114387.2:c.320+33G>C MANE Select	NP_001107859.1:n.320+33G>C
NM_182606.4:c.329+33G>C	NP_872412.3:n.329+33G>C