Canonical Allele Identifier: CA512424012
Gene: TMPRSS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43810040C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389931C>A , CM000683.2:g.42389931C>A GRCh38
NC_000021.8:g.43810040C>A , CM000683.1:g.43810040C>A GRCh37
NC_000021.7:g.42683109C>A NCBI36
NG_011629.1:g.11161G>T
NG_011629.2:g.11161G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.201G>T ENSP00000411013.3:p.Leu67=
ENST00000644384.2:c.201G>T MANE Select ENSP00000494414.1:p.Leu67=
ENST00000652415.1:c.201G>T ENSP00000498756.1:p.Leu67=
ENST00000291532.7:c.201G>T ENSP00000291532.3:p.Leu67=
ENST00000398397.3:c.201G>T ENSP00000381434.3:p.Leu67=
ENST00000398405.5:c.195G>T ENSP00000381442.1:p.Leu65=
ENST00000433957.6:c.201G>T ENSP00000411013.2:p.Leu67=
ENST00000482761.1:n.488G>T
NM_001256317.1:c.201G>T NP_001243246.1:p.Leu67=
NM_024022.2:c.201G>T NP_076927.1:p.Leu67=
NM_032405.1:c.201G>T NP_115781.1:p.Leu67=
NR_046020.1:n.1157G>T
NM_001256317.2:c.201G>T NP_001243246.1:p.Leu67=
NM_024022.3:c.201G>T NP_076927.1:p.Leu67=
NM_032405.2:c.201G>T NP_115781.1:p.Leu67=
NM_001256317.3:c.201G>T MANE Select NP_001243246.1:p.Leu67=
NM_024022.4:c.201G>T NP_076927.1:p.Leu67=