Canonical Allele Identifier: CA637901489

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1458317764
• gnomAD v2: 21-43792566-A-G
• gnomAD v4: 21-42372457-A-G
• MyVariant Identifiers: chr21:g.43792566A>G (hg19) ; chr21:g.42372457A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372457A>G , CM000683.2:g.42372457A>G	GRCh38
NC_000021.8:g.43792566A>G , CM000683.1:g.43792566A>G	GRCh37
NC_000021.7:g.42665635A>G	NCBI36
NG_011629.1:g.28635T>C
NG_011629.2:g.28635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*305T>C	ENSP00000411013.3:n.*305T>C
ENST00000644384.2:c.*305T>C MANE Select	ENSP00000494414.1:n.*305T>C
ENST00000652415.1:c.*305T>C	ENSP00000498756.1:n.*305T>C
ENST00000291532.7:c.*305T>C	ENSP00000291532.3:n.*305T>C
ENST00000398405.5:c.*305T>C	ENSP00000381442.1:n.*305T>C
ENST00000433957.6:c.*305T>C	ENSP00000411013.2:n.*305T>C
ENST00000474596.5:n.1538T>C
ENST00000476848.5:n.2402T>C
ENST00000482761.1:n.1957T>C
NM_001256317.1:c.*305T>C	NP_001243246.1:n.*305T>C
NM_024022.2:c.*305T>C	NP_076927.1:n.*305T>C
NM_032404.2:c.*305T>C	NP_115780.1:n.*305T>C
NR_046020.1:n.2626T>C
NM_001256317.2:c.*305T>C	NP_001243246.1:n.*305T>C
NM_024022.3:c.*305T>C	NP_076927.1:n.*305T>C
NM_001256317.3:c.*305T>C MANE Select	NP_001243246.1:n.*305T>C
NM_024022.4:c.*305T>C	NP_076927.1:n.*305T>C
NM_032404.3:c.*305T>C	NP_115780.1:n.*305T>C