Canonical Allele Identifier: CA2390778458

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs2052548713

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382323G>A , CM000683.2:g.42382323G>A	GRCh38
NC_000021.8:g.43802432G>A , CM000683.1:g.43802432G>A	GRCh37
NC_000021.7:g.42675501G>A	NCBI36
NG_011629.1:g.18769C>T
NG_011629.2:g.18769C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.783-89C>T	ENSP00000411013.3:n.783-89C>T
ENST00000644384.2:c.783-89C>T MANE Select	ENSP00000494414.1:n.783-89C>T
ENST00000652415.1:c.783-89C>T	ENSP00000498756.1:n.783-89C>T
ENST00000291532.7:c.783-89C>T	ENSP00000291532.3:n.783-89C>T
ENST00000398397.3:c.783-89C>T	ENSP00000381434.3:n.783-89C>T
ENST00000398405.5:c.777-89C>T	ENSP00000381442.1:n.777-89C>T
ENST00000433957.6:c.783-89C>T	ENSP00000411013.2:n.783-89C>T
ENST00000474596.5:n.651-89C>T
ENST00000476848.5:n.1429C>T
ENST00000478680.1:n.60-89C>T
ENST00000482761.1:n.1070-89C>T
NM_001256317.1:c.783-89C>T	NP_001243246.1:n.783-89C>T
NM_024022.2:c.783-89C>T	NP_076927.1:n.783-89C>T
NM_032404.2:c.402-89C>T	NP_115780.1:n.402-89C>T
NM_032405.1:c.783-89C>T	NP_115781.1:n.783-89C>T
NR_046020.1:n.1739-89C>T
NM_001256317.2:c.783-89C>T	NP_001243246.1:n.783-89C>T
NM_024022.3:c.783-89C>T	NP_076927.1:n.783-89C>T
NM_032405.2:c.783-89C>T	NP_115781.1:n.783-89C>T
NM_001256317.3:c.783-89C>T MANE Select	NP_001243246.1:n.783-89C>T
NM_024022.4:c.783-89C>T	NP_076927.1:n.783-89C>T
NM_032404.3:c.402-89C>T	NP_115780.1:n.402-89C>T