Canonical Allele Identifier: CA410374745

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43805521A>G (hg19) ; chr21:g.42385412A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.569T>C	ENSP00000411013.3:p.Val190Ala
ENST00000644384.2:c.569T>C MANE Select	ENSP00000494414.1:p.Val190Ala
ENST00000652415.1:c.569T>C	ENSP00000498756.1:p.Val190Ala
ENST00000291532.7:c.569T>C	ENSP00000291532.3:p.Val190Ala
ENST00000398397.3:c.569T>C	ENSP00000381434.3:p.Val190Ala
ENST00000398405.5:c.563T>C	ENSP00000381442.1:p.Val188Ala
ENST00000433957.6:c.569T>C	ENSP00000411013.2:p.Val190Ala
ENST00000474596.5:n.437T>C
ENST00000482761.1:n.856T>C
NM_001256317.1:c.569T>C	NP_001243246.1:p.Val190Ala
NM_024022.2:c.569T>C	NP_076927.1:p.Val190Ala
NM_032404.2:c.188T>C	NP_115780.1:p.Val63Ala
NM_032405.1:c.569T>C	NP_115781.1:p.Val190Ala
NR_046020.1:n.1525T>C
NM_001256317.2:c.569T>C	NP_001243246.1:p.Val190Ala
NM_024022.3:c.569T>C	NP_076927.1:p.Val190Ala
NM_032405.2:c.569T>C	NP_115781.1:p.Val190Ala
NM_001256317.3:c.569T>C MANE Select	NP_001243246.1:p.Val190Ala
NM_024022.4:c.569T>C	NP_076927.1:p.Val190Ala
NM_032404.3:c.188T>C	NP_115780.1:p.Val63Ala