Canonical Allele Identifier: CA512423934
Gene: TMPRSS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43809117T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389008T>G , CM000683.2:g.42389008T>G GRCh38
NC_000021.8:g.43809117T>G , CM000683.1:g.43809117T>G GRCh37
NC_000021.7:g.42682186T>G NCBI36
NG_011629.1:g.12084A>C
NG_011629.2:g.12084A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.243A>C ENSP00000411013.3:p.Ser81=
ENST00000644384.2:c.243A>C MANE Select ENSP00000494414.1:p.Ser81=
ENST00000652415.1:c.243A>C ENSP00000498756.1:p.Ser81=
ENST00000291532.7:c.243A>C ENSP00000291532.3:p.Ser81=
ENST00000398397.3:c.243A>C ENSP00000381434.3:p.Ser81=
ENST00000398405.5:c.237A>C ENSP00000381442.1:p.Ser79=
ENST00000433957.6:c.243A>C ENSP00000411013.2:p.Ser81=
ENST00000474596.5:n.111A>C
ENST00000482761.1:n.530A>C
NM_001256317.1:c.243A>C NP_001243246.1:p.Ser81=
NM_024022.2:c.243A>C NP_076927.1:p.Ser81=
NM_032404.2:c.-139A>C NP_115780.1:n.-139A>C
NM_032405.1:c.243A>C NP_115781.1:p.Ser81=
NR_046020.1:n.1199A>C
NM_001256317.2:c.243A>C NP_001243246.1:p.Ser81=
NM_024022.3:c.243A>C NP_076927.1:p.Ser81=
NM_032405.2:c.243A>C NP_115781.1:p.Ser81=
NM_001256317.3:c.243A>C MANE Select NP_001243246.1:p.Ser81=
NM_024022.4:c.243A>C NP_076927.1:p.Ser81=
NM_032404.3:c.-139A>C NP_115780.1:n.-139A>C