Canonical Allele Identifier: CA410376009

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43810129C>T (hg19) ; chr21:g.42390020C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42390020C>T , CM000683.2:g.42390020C>T	GRCh38
NC_000021.8:g.43810129C>T , CM000683.1:g.43810129C>T	GRCh37
NC_000021.7:g.42683198C>T	NCBI36
NG_011629.1:g.11072G>A
NG_011629.2:g.11072G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.112G>A	ENSP00000411013.3:p.Ala38Thr
ENST00000644384.2:c.112G>A MANE Select	ENSP00000494414.1:p.Ala38Thr
ENST00000652415.1:c.112G>A	ENSP00000498756.1:p.Ala38Thr
ENST00000291532.7:c.112G>A	ENSP00000291532.3:p.Ala38Thr
ENST00000398397.3:c.112G>A	ENSP00000381434.3:p.Ala38Thr
ENST00000398405.5:c.106G>A	ENSP00000381442.1:p.Ala36Thr
ENST00000433957.6:c.112G>A	ENSP00000411013.2:p.Ala38Thr
ENST00000482761.1:n.399G>A
NM_001256317.1:c.112G>A	NP_001243246.1:p.Ala38Thr
NM_024022.2:c.112G>A	NP_076927.1:p.Ala38Thr
NM_032405.1:c.112G>A	NP_115781.1:p.Ala38Thr
NR_046020.1:n.1068G>A
NM_001256317.2:c.112G>A	NP_001243246.1:p.Ala38Thr
NM_024022.3:c.112G>A	NP_076927.1:p.Ala38Thr
NM_032405.2:c.112G>A	NP_115781.1:p.Ala38Thr
NM_001256317.3:c.112G>A MANE Select	NP_001243246.1:p.Ala38Thr
NM_024022.4:c.112G>A	NP_076927.1:p.Ala38Thr