Canonical Allele Identifier: CA1022593812

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs2052694522
• gnomAD v3: 21-42389314-T-A
• gnomAD v4: 21-42389314-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42389314T>A , CM000683.2:g.42389314T>A	GRCh38
NC_000021.8:g.43809423T>A , CM000683.1:g.43809423T>A	GRCh37
NC_000021.7:g.42682492T>A	NCBI36
NG_011629.1:g.11778A>T
NG_011629.2:g.11778A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.206-269A>T	ENSP00000411013.3:n.206-269A>T
ENST00000644384.2:c.206-269A>T MANE Select	ENSP00000494414.1:n.206-269A>T
ENST00000652415.1:c.206-269A>T	ENSP00000498756.1:n.206-269A>T
ENST00000291532.7:c.206-269A>T	ENSP00000291532.3:n.206-269A>T
ENST00000398397.3:c.206-269A>T	ENSP00000381434.3:n.206-269A>T
ENST00000398405.5:c.200-269A>T	ENSP00000381442.1:n.200-269A>T
ENST00000433957.6:c.206-269A>T	ENSP00000411013.2:n.206-269A>T
ENST00000482761.1:n.493-269A>T
NM_001256317.1:c.206-269A>T	NP_001243246.1:n.206-269A>T
NM_024022.2:c.206-269A>T	NP_076927.1:n.206-269A>T
NM_032405.1:c.206-269A>T	NP_115781.1:n.206-269A>T
NR_046020.1:n.1162-269A>T
NM_001256317.2:c.206-269A>T	NP_001243246.1:n.206-269A>T
NM_024022.3:c.206-269A>T	NP_076927.1:n.206-269A>T
NM_032405.2:c.206-269A>T	NP_115781.1:n.206-269A>T
NM_001256317.3:c.206-269A>T MANE Select	NP_001243246.1:n.206-269A>T
NM_024022.4:c.206-269A>T	NP_076927.1:n.206-269A>T