Canonical Allele Identifier: CA2654681071

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42388828-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42388833dup , CM000683.2:g.42388833dup	GRCh38
NC_000021.8:g.43808942dup , CM000683.1:g.43808942dup	GRCh37
NC_000021.7:g.42682011dup	NCBI36
NG_011629.1:g.12263dup
NG_011629.2:g.12263dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.322+100dup	ENSP00000411013.3:n.322+100dup
ENST00000644384.2:c.322+100dup MANE Select	ENSP00000494414.1:n.322+100dup
ENST00000652415.1:c.322+100dup	ENSP00000498756.1:n.322+100dup
ENST00000291532.7:c.322+100dup	ENSP00000291532.3:n.322+100dup
ENST00000398397.3:c.322+100dup	ENSP00000381434.3:n.322+100dup
ENST00000398405.5:c.316+100dup	ENSP00000381442.1:n.316+100dup
ENST00000433957.6:c.322+100dup	ENSP00000411013.2:n.322+100dup
ENST00000474596.5:n.190+100dup
ENST00000482761.1:n.609+100dup
NM_001256317.1:c.322+100dup	NP_001243246.1:n.322+100dup
NM_024022.2:c.322+100dup	NP_076927.1:n.322+100dup
NM_032404.2:c.-60+100dup	NP_115780.1:n.-60+100dup
NM_032405.1:c.322+100dup	NP_115781.1:n.322+100dup
NR_046020.1:n.1278+100dup
NM_001256317.2:c.322+100dup	NP_001243246.1:n.322+100dup
NM_024022.3:c.322+100dup	NP_076927.1:n.322+100dup
NM_032405.2:c.322+100dup	NP_115781.1:n.322+100dup
NM_001256317.3:c.322+100dup MANE Select	NP_001243246.1:n.322+100dup
NM_024022.4:c.322+100dup	NP_076927.1:n.322+100dup
NM_032404.3:c.-60+100dup	NP_115780.1:n.-60+100dup