Canonical Allele Identifier: CA321548735

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs949061409
• gnomAD v3: 21-42388844-T-G
• gnomAD v4: 21-42388844-T-G
• MyVariant Identifiers: chr21:g.43808953T>G (hg19) ; chr21:g.42388844T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42388844T>G , CM000683.2:g.42388844T>G	GRCh38
NC_000021.8:g.43808953T>G , CM000683.1:g.43808953T>G	GRCh37
NC_000021.7:g.42682022T>G	NCBI36
NG_011629.1:g.12248A>C
NG_011629.2:g.12248A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.322+85A>C	ENSP00000411013.3:n.322+85A>C
ENST00000644384.2:c.322+85A>C MANE Select	ENSP00000494414.1:n.322+85A>C
ENST00000652415.1:c.322+85A>C	ENSP00000498756.1:n.322+85A>C
ENST00000291532.7:c.322+85A>C	ENSP00000291532.3:n.322+85A>C
ENST00000398397.3:c.322+85A>C	ENSP00000381434.3:n.322+85A>C
ENST00000398405.5:c.316+85A>C	ENSP00000381442.1:n.316+85A>C
ENST00000433957.6:c.322+85A>C	ENSP00000411013.2:n.322+85A>C
ENST00000474596.5:n.190+85A>C
ENST00000482761.1:n.609+85A>C
NM_001256317.1:c.322+85A>C	NP_001243246.1:n.322+85A>C
NM_024022.2:c.322+85A>C	NP_076927.1:n.322+85A>C
NM_032404.2:c.-60+85A>C	NP_115780.1:n.-60+85A>C
NM_032405.1:c.322+85A>C	NP_115781.1:n.322+85A>C
NR_046020.1:n.1278+85A>C
NM_001256317.2:c.322+85A>C	NP_001243246.1:n.322+85A>C
NM_024022.3:c.322+85A>C	NP_076927.1:n.322+85A>C
NM_032405.2:c.322+85A>C	NP_115781.1:n.322+85A>C
NM_001256317.3:c.322+85A>C MANE Select	NP_001243246.1:n.322+85A>C
NM_024022.4:c.322+85A>C	NP_076927.1:n.322+85A>C
NM_032404.3:c.-60+85A>C	NP_115780.1:n.-60+85A>C