Canonical Allele Identifier: CA2654678363

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42372501-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372501A>G , CM000683.2:g.42372501A>G	GRCh38
NC_000021.8:g.43792610A>G , CM000683.1:g.43792610A>G	GRCh37
NC_000021.7:g.42665679A>G	NCBI36
NG_011629.1:g.28591T>C
NG_011629.2:g.28591T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.*261T>C	ENSP00000411013.3:n.*261T>C
ENST00000644384.2:c.*261T>C MANE Select	ENSP00000494414.1:n.*261T>C
ENST00000652415.1:c.*261T>C	ENSP00000498756.1:n.*261T>C
ENST00000291532.7:c.*261T>C	ENSP00000291532.3:n.*261T>C
ENST00000398405.5:c.*261T>C	ENSP00000381442.1:n.*261T>C
ENST00000433957.6:c.*261T>C	ENSP00000411013.2:n.*261T>C
ENST00000474596.5:n.1494T>C
ENST00000476848.5:n.2358T>C
ENST00000482761.1:n.1913T>C
NM_001256317.1:c.*261T>C	NP_001243246.1:n.*261T>C
NM_024022.2:c.*261T>C	NP_076927.1:n.*261T>C
NM_032404.2:c.*261T>C	NP_115780.1:n.*261T>C
NR_046020.1:n.2582T>C
NM_001256317.2:c.*261T>C	NP_001243246.1:n.*261T>C
NM_024022.3:c.*261T>C	NP_076927.1:n.*261T>C
NM_001256317.3:c.*261T>C MANE Select	NP_001243246.1:n.*261T>C
NM_024022.4:c.*261T>C	NP_076927.1:n.*261T>C
NM_032404.3:c.*261T>C	NP_115780.1:n.*261T>C