Canonical Allele Identifier: CA512423915

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43809089G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42388980G>T , CM000683.2:g.42388980G>T	GRCh38
NC_000021.8:g.43809089G>T , CM000683.1:g.43809089G>T	GRCh37
NC_000021.7:g.42682158G>T	NCBI36
NG_011629.1:g.12112C>A
NG_011629.2:g.12112C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.271C>A	ENSP00000411013.3:p.Arg91=
ENST00000644384.2:c.271C>A MANE Select	ENSP00000494414.1:p.Arg91=
ENST00000652415.1:c.271C>A	ENSP00000498756.1:p.Arg91=
ENST00000291532.7:c.271C>A	ENSP00000291532.3:p.Arg91=
ENST00000398397.3:c.271C>A	ENSP00000381434.3:p.Arg91=
ENST00000398405.5:c.265C>A	ENSP00000381442.1:p.Arg89=
ENST00000433957.6:c.271C>A	ENSP00000411013.2:p.Arg91=
ENST00000474596.5:n.139C>A
ENST00000482761.1:n.558C>A
NM_001256317.1:c.271C>A	NP_001243246.1:p.Arg91=
NM_024022.2:c.271C>A	NP_076927.1:p.Arg91=
NM_032404.2:c.-111C>A	NP_115780.1:n.-111C>A
NM_032405.1:c.271C>A	NP_115781.1:p.Arg91=
NR_046020.1:n.1227C>A
NM_001256317.2:c.271C>A	NP_001243246.1:p.Arg91=
NM_024022.3:c.271C>A	NP_076927.1:p.Arg91=
NM_032405.2:c.271C>A	NP_115781.1:p.Arg91=
NM_001256317.3:c.271C>A MANE Select	NP_001243246.1:p.Arg91=
NM_024022.4:c.271C>A	NP_076927.1:p.Arg91=
NM_032404.3:c.-111C>A	NP_115780.1:n.-111C>A