Canonical Allele Identifier: CA410374746

Gene: TMPRSS3

Linked Data

• gnomAD v3: 21-42385412-A-T
• gnomAD v4: 21-42385412-A-T
• MyVariant Identifiers: chr21:g.43805521A>T (hg19) ; chr21:g.42385412A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42385412A>T , CM000683.2:g.42385412A>T	GRCh38
NC_000021.8:g.43805521A>T , CM000683.1:g.43805521A>T	GRCh37
NC_000021.7:g.42678590A>T	NCBI36
NG_011629.1:g.15680T>A
NG_011629.2:g.15680T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.569T>A	ENSP00000411013.3:p.Val190Glu
ENST00000644384.2:c.569T>A MANE Select	ENSP00000494414.1:p.Val190Glu
ENST00000652415.1:c.569T>A	ENSP00000498756.1:p.Val190Glu
ENST00000291532.7:c.569T>A	ENSP00000291532.3:p.Val190Glu
ENST00000398397.3:c.569T>A	ENSP00000381434.3:p.Val190Glu
ENST00000398405.5:c.563T>A	ENSP00000381442.1:p.Val188Glu
ENST00000433957.6:c.569T>A	ENSP00000411013.2:p.Val190Glu
ENST00000474596.5:n.437T>A
ENST00000482761.1:n.856T>A
NM_001256317.1:c.569T>A	NP_001243246.1:p.Val190Glu
NM_024022.2:c.569T>A	NP_076927.1:p.Val190Glu
NM_032404.2:c.188T>A	NP_115780.1:p.Val63Glu
NM_032405.1:c.569T>A	NP_115781.1:p.Val190Glu
NR_046020.1:n.1525T>A
NM_001256317.2:c.569T>A	NP_001243246.1:p.Val190Glu
NM_024022.3:c.569T>A	NP_076927.1:p.Val190Glu
NM_032405.2:c.569T>A	NP_115781.1:p.Val190Glu
NM_001256317.3:c.569T>A MANE Select	NP_001243246.1:p.Val190Glu
NM_024022.4:c.569T>A	NP_076927.1:p.Val190Glu
NM_032404.3:c.188T>A	NP_115780.1:p.Val63Glu