Canonical Allele Identifier: CA10042162

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs763182738
• ExAC: 21:43792600 C / CGGA
• gnomAD v2: 21-43792600-C-CGGA
• gnomAD v3: 21-42372491-C-CGGA
• gnomAD v4: 21-42372491-C-CGGA
• MyVariant Identifiers: chr21:g.43792600_43792601insGGA (hg19) ; chr21:g.42372491_42372492insGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372494_42372496dup , CM000683.2:g.42372494_42372496dup	GRCh38
NC_000021.8:g.43792603_43792605dup , CM000683.1:g.43792603_43792605dup	GRCh37
NC_000021.7:g.42665672_42665674dup	NCBI36
NG_011629.1:g.28598_28600dup
NG_011629.2:g.28598_28600dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.*268_*270dup	ENSP00000411013.3:n.*268_*270dup
ENST00000644384.2:c.*268_*270dup MANE Select	ENSP00000494414.1:n.*268_*270dup
ENST00000652415.1:c.*268_*270dup	ENSP00000498756.1:n.*268_*270dup
ENST00000291532.7:c.*268_*270dup	ENSP00000291532.3:n.*268_*270dup
ENST00000398405.5:c.*268_*270dup	ENSP00000381442.1:n.*268_*270dup
ENST00000433957.6:c.*268_*270dup	ENSP00000411013.2:n.*268_*270dup
ENST00000474596.5:n.1501_1503dup
ENST00000476848.5:n.2365_2367dup
ENST00000482761.1:n.1920_1922dup
NM_001256317.1:c.*268_*270dup	NP_001243246.1:n.*268_*270dup
NM_024022.2:c.*268_*270dup	NP_076927.1:n.*268_*270dup
NM_032404.2:c.*268_*270dup	NP_115780.1:n.*268_*270dup
NR_046020.1:n.2589_2591dup
NM_001256317.2:c.*268_*270dup	NP_001243246.1:n.*268_*270dup
NM_024022.3:c.*268_*270dup	NP_076927.1:n.*268_*270dup
NM_001256317.3:c.*268_*270dup MANE Select	NP_001243246.1:n.*268_*270dup
NM_024022.4:c.*268_*270dup	NP_076927.1:n.*268_*270dup
NM_032404.3:c.*268_*270dup	NP_115780.1:n.*268_*270dup