Canonical Allele Identifier: CA410375183

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43805604C>A (hg19) ; chr21:g.42385495C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42385495C>A , CM000683.2:g.42385495C>A	GRCh38
NC_000021.8:g.43805604C>A , CM000683.1:g.43805604C>A	GRCh37
NC_000021.7:g.42678673C>A	NCBI36
NG_011629.1:g.15597G>T
NG_011629.2:g.15597G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.486G>T	ENSP00000411013.3:p.Glu162Asp
ENST00000644384.2:c.486G>T MANE Select	ENSP00000494414.1:p.Glu162Asp
ENST00000652415.1:c.486G>T	ENSP00000498756.1:p.Glu162Asp
ENST00000291532.7:c.486G>T	ENSP00000291532.3:p.Glu162Asp
ENST00000398397.3:c.486G>T	ENSP00000381434.3:p.Glu162Asp
ENST00000398405.5:c.480G>T	ENSP00000381442.1:p.Glu160Asp
ENST00000433957.6:c.486G>T	ENSP00000411013.2:p.Glu162Asp
ENST00000474596.5:n.354G>T
ENST00000482761.1:n.773G>T
NM_001256317.1:c.486G>T	NP_001243246.1:p.Glu162Asp
NM_024022.2:c.486G>T	NP_076927.1:p.Glu162Asp
NM_032404.2:c.105G>T	NP_115780.1:p.Glu35Asp
NM_032405.1:c.486G>T	NP_115781.1:p.Glu162Asp
NR_046020.1:n.1442G>T
NM_001256317.2:c.486G>T	NP_001243246.1:p.Glu162Asp
NM_024022.3:c.486G>T	NP_076927.1:p.Glu162Asp
NM_032405.2:c.486G>T	NP_115781.1:p.Glu162Asp
NM_001256317.3:c.486G>T MANE Select	NP_001243246.1:p.Glu162Asp
NM_024022.4:c.486G>T	NP_076927.1:p.Glu162Asp
NM_032404.3:c.105G>T	NP_115780.1:p.Glu35Asp