Canonical Allele Identifier: CA10653641

Gene: TMPRSS3

Linked Data

• ClinVar Variation Id: 340050
• ClinVar RCV Id: RCV000275211
• dbSNP Id: rs886057092
• MyVariant Identifiers: chr21:g.43792474G>T (hg19) ; chr21:g.42372365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372365G>T , CM000683.2:g.42372365G>T	GRCh38
NC_000021.8:g.43792474G>T , CM000683.1:g.43792474G>T	GRCh37
NC_000021.7:g.42665543G>T	NCBI36
NG_011629.1:g.28727C>A
NG_011629.2:g.28727C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*397C>A	ENSP00000411013.3:n.*397C>A
ENST00000644384.2:c.*397C>A MANE Select	ENSP00000494414.1:n.*397C>A
ENST00000652415.1:c.*397C>A	ENSP00000498756.1:n.*397C>A
ENST00000291532.7:c.*397C>A	ENSP00000291532.3:n.*397C>A
ENST00000398405.5:c.*397C>A	ENSP00000381442.1:n.*397C>A
ENST00000433957.6:c.*397C>A	ENSP00000411013.2:n.*397C>A
ENST00000474596.5:n.1630C>A
ENST00000476848.5:n.2494C>A
ENST00000482761.1:n.2049C>A
NM_001256317.1:c.*397C>A	NP_001243246.1:n.*397C>A
NM_024022.2:c.*397C>A	NP_076927.1:n.*397C>A
NM_032404.2:c.*397C>A	NP_115780.1:n.*397C>A
NR_046020.1:n.2718C>A
NM_001256317.2:c.*397C>A	NP_001243246.1:n.*397C>A
NM_024022.3:c.*397C>A	NP_076927.1:n.*397C>A
NM_001256317.3:c.*397C>A MANE Select	NP_001243246.1:n.*397C>A
NM_024022.4:c.*397C>A	NP_076927.1:n.*397C>A
NM_032404.3:c.*397C>A	NP_115780.1:n.*397C>A