Canonical Allele Identifier: CA512423122

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43802328C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382219C>T , CM000683.2:g.42382219C>T	GRCh38
NC_000021.8:g.43802328C>T , CM000683.1:g.43802328C>T	GRCh37
NC_000021.7:g.42675397C>T	NCBI36
NG_011629.1:g.18873G>A
NG_011629.2:g.18873G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.798G>A	ENSP00000411013.3:p.Lys266=
ENST00000644384.2:c.798G>A MANE Select	ENSP00000494414.1:p.Lys266=
ENST00000652415.1:c.798G>A	ENSP00000498756.1:p.Lys266=
ENST00000291532.7:c.798G>A	ENSP00000291532.3:p.Lys266=
ENST00000398397.3:c.798G>A	ENSP00000381434.3:p.Lys266=
ENST00000398405.5:c.792G>A	ENSP00000381442.1:p.Lys264=
ENST00000433957.6:c.798G>A	ENSP00000411013.2:p.Lys266=
ENST00000474596.5:n.666G>A
ENST00000476848.5:n.1533G>A
ENST00000478680.1:n.75G>A
ENST00000482761.1:n.1085G>A
NM_001256317.1:c.798G>A	NP_001243246.1:p.Lys266=
NM_024022.2:c.798G>A	NP_076927.1:p.Lys266=
NM_032404.2:c.417G>A	NP_115780.1:p.Lys139=
NM_032405.1:c.798G>A	NP_115781.1:p.Lys266=
NR_046020.1:n.1754G>A
NM_001256317.2:c.798G>A	NP_001243246.1:p.Lys266=
NM_024022.3:c.798G>A	NP_076927.1:p.Lys266=
NM_032405.2:c.798G>A	NP_115781.1:p.Lys266=
NM_001256317.3:c.798G>A MANE Select	NP_001243246.1:p.Lys266=
NM_024022.4:c.798G>A	NP_076927.1:p.Lys266=
NM_032404.3:c.417G>A	NP_115780.1:p.Lys139=