Canonical Allele Identifier: CA410372560

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43802245C>G (hg19) ; chr21:g.42382136C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382136C>G , CM000683.2:g.42382136C>G	GRCh38
NC_000021.8:g.43802245C>G , CM000683.1:g.43802245C>G	GRCh37
NC_000021.7:g.42675314C>G	NCBI36
NG_011629.1:g.18956G>C
NG_011629.2:g.18956G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.881G>C	ENSP00000411013.3:p.Ser294Thr
ENST00000644384.2:c.881G>C MANE Select	ENSP00000494414.1:p.Ser294Thr
ENST00000652415.1:c.881G>C	ENSP00000498756.1:p.Ser294Thr
ENST00000291532.7:c.881G>C	ENSP00000291532.3:p.Ser294Thr
ENST00000398397.3:c.881G>C	ENSP00000381434.3:p.Ser294Thr
ENST00000398405.5:c.875G>C	ENSP00000381442.1:p.Ser292Thr
ENST00000433957.6:c.881G>C	ENSP00000411013.2:p.Ser294Thr
ENST00000474596.5:n.749G>C
ENST00000476848.5:n.1616G>C
ENST00000478680.1:n.158G>C
ENST00000482761.1:n.1168G>C
NM_001256317.1:c.881G>C	NP_001243246.1:p.Ser294Thr
NM_024022.2:c.881G>C	NP_076927.1:p.Ser294Thr
NM_032404.2:c.500G>C	NP_115780.1:p.Ser167Thr
NM_032405.1:c.881G>C	NP_115781.1:p.Ser294Thr
NR_046020.1:n.1837G>C
NM_001256317.2:c.881G>C	NP_001243246.1:p.Ser294Thr
NM_024022.3:c.881G>C	NP_076927.1:p.Ser294Thr
NM_032405.2:c.881G>C	NP_115781.1:p.Ser294Thr
NM_001256317.3:c.881G>C MANE Select	NP_001243246.1:p.Ser294Thr
NM_024022.4:c.881G>C	NP_076927.1:p.Ser294Thr
NM_032404.3:c.500G>C	NP_115780.1:p.Ser167Thr