Canonical Allele Identifier: CA14880880
Community Standard Title: NM_001256317.3(TMPRSS3):c.1049-121A>T
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42376804T>A , CM000683.2:g.42376804T>A GRCh38
NC_000021.8:g.43796913T>A , CM000683.1:g.43796913T>A GRCh37
NC_000021.7:g.42669982T>A NCBI36
NG_011629.1:g.24288A>T
NG_011629.2:g.24288A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001256317.3:c.1049-121A>T MANE Select NP_001243246.1:n.1049-121A>T
ENST00000644384.2:c.1049-121A>T MANE Select ENSP00000494414.1:n.1049-121A>T
NM_001256317.1:c.1049-121A>T NP_001243246.1:n.1049-121A>T
NM_001256317.2:c.1049-121A>T NP_001243246.1:n.1049-121A>T
NM_024022.2:c.1049-118A>T NP_076927.1:n.1049-118A>T
NM_024022.3:c.1049-118A>T NP_076927.1:n.1049-118A>T
NM_024022.4:c.1049-118A>T NP_076927.1:n.1049-118A>T
NM_032404.2:c.668-118A>T NP_115780.1:n.668-118A>T
NM_032404.3:c.668-118A>T NP_115780.1:n.668-118A>T
NR_046020.1:n.2005-118A>T
ENST00000291532.7:c.1049-118A>T ENSP00000291532.3:n.1049-118A>T
ENST00000398405.5:c.1043-121A>T ENSP00000381442.1:n.1043-121A>T
ENST00000433957.6:c.1049-121A>T ENSP00000411013.2:n.1049-121A>T
ENST00000433957.7:c.1049-118A>T ENSP00000411013.3:n.1049-118A>T
ENST00000474596.5:n.917-118A>T
ENST00000476848.5:n.1784-121A>T
ENST00000482761.1:n.1336-118A>T
ENST00000652415.1:c.1049-121A>T ENSP00000498756.1:n.1049-121A>T