Canonical Allele Identifier: CA410368498

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42375720A>C , CM000683.2:g.42375720A>C	GRCh38
NC_000021.8:g.43795829A>C , CM000683.1:g.43795829A>C	GRCh37
NC_000021.7:g.42668898A>C	NCBI36
NG_011629.1:g.25372T>G
NG_011629.2:g.25372T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001256317.3:c.1340T>G MANE Select	NP_001243246.1:p.Met447Arg
ENST00000644384.2:c.1340T>G MANE Select	ENSP00000494414.1:p.Met447Arg
NM_001256317.1:c.1340T>G	NP_001243246.1:p.Met447Arg
NM_001256317.2:c.1340T>G	NP_001243246.1:p.Met447Arg
NM_024022.2:c.1343T>G	NP_076927.1:p.Met448Arg
NM_024022.3:c.1343T>G	NP_076927.1:p.Met448Arg
NM_024022.4:c.1343T>G	NP_076927.1:p.Met448Arg
NM_032404.2:c.962T>G	NP_115780.1:p.Met321Arg
NM_032404.3:c.962T>G	NP_115780.1:p.Met321Arg
NR_046020.1:n.2299T>G
ENST00000291532.7:c.1343T>G	ENSP00000291532.3:p.Met448Arg
ENST00000398405.5:c.1334T>G	ENSP00000381442.1:p.Met445Arg
ENST00000433957.6:c.1340T>G	ENSP00000411013.2:p.Met447Arg
ENST00000433957.7:c.1343T>G	ENSP00000411013.3:p.Met448Arg
ENST00000474596.5:n.1211T>G
ENST00000476848.5:n.2075T>G
ENST00000482761.1:n.1630T>G
ENST00000652415.1:c.1340T>G	ENSP00000498756.1:p.Met447Arg