Canonical Allele Identifier: CA2654681100

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42388852-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42388856del , CM000683.2:g.42388856del	GRCh38
NC_000021.8:g.43808965del , CM000683.1:g.43808965del	GRCh37
NC_000021.7:g.42682034del	NCBI36
NG_011629.1:g.12239del
NG_011629.2:g.12239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.322+76del	ENSP00000411013.3:n.322+76del
ENST00000644384.2:c.322+76del MANE Select	ENSP00000494414.1:n.322+76del
ENST00000652415.1:c.322+76del	ENSP00000498756.1:n.322+76del
ENST00000291532.7:c.322+76del	ENSP00000291532.3:n.322+76del
ENST00000398397.3:c.322+76del	ENSP00000381434.3:n.322+76del
ENST00000398405.5:c.316+76del	ENSP00000381442.1:n.316+76del
ENST00000433957.6:c.322+76del	ENSP00000411013.2:n.322+76del
ENST00000474596.5:n.190+76del
ENST00000482761.1:n.609+76del
NM_001256317.1:c.322+76del	NP_001243246.1:n.322+76del
NM_024022.2:c.322+76del	NP_076927.1:n.322+76del
NM_032404.2:c.-60+76del	NP_115780.1:n.-60+76del
NM_032405.1:c.322+76del	NP_115781.1:n.322+76del
NR_046020.1:n.1278+76del
NM_001256317.2:c.322+76del	NP_001243246.1:n.322+76del
NM_024022.3:c.322+76del	NP_076927.1:n.322+76del
NM_032405.2:c.322+76del	NP_115781.1:n.322+76del
NM_001256317.3:c.322+76del MANE Select	NP_001243246.1:n.322+76del
NM_024022.4:c.322+76del	NP_076927.1:n.322+76del
NM_032404.3:c.-60+76del	NP_115780.1:n.-60+76del