Canonical Allele Identifier: CA2583996218

Gene: TMPRSS9

Linked Data

• gnomAD v4: 19-2410493-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2410498dup , CM000681.2:g.2410498dup	GRCh38
NC_000019.9:g.2410496dup , CM000681.1:g.2410496dup	GRCh37
NC_000019.8:g.2361496dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696167.1:c.1254+104dup MANE Select	ENSP00000512457.1:n.1254+104dup
ENST00000648592.1:c.1254+104dup	ENSP00000498031.1:n.1254+104dup
ENST00000649857.1:c.1152+104dup	ENSP00000497651.1:n.1152+104dup
ENST00000332578.7:c.1152+104dup	ENSP00000330264.2:n.1152+104dup
ENST00000395264.3:n.1269+104dup
ENST00000613480.1:c.1152+104dup	ENSP00000482424.1:n.1152+104dup
NM_182973.1:c.1152+104dup	NP_892018.1:n.1152+104dup
XM_011527978.1:c.1254+104dup	XP_011526280.1:n.1254+104dup
XM_011527979.1:c.1155+104dup	XP_011526281.1:n.1155+104dup
XM_011527980.1:c.45+104dup	XP_011526282.1:n.45+104dup
XM_011527981.1:c.1254+104dup	XP_011526283.1:n.1254+104dup
XM_011527983.1:c.1254+104dup	XP_011526285.1:n.1254+104dup
NM_182973.2:c.1152+104dup	NP_892018.1:n.1152+104dup
XM_011527978.2:c.1254+104dup	XP_011526280.1:n.1254+104dup
NM_001385642.1:c.558+104dup	NP_001372571.1:n.558+104dup
NM_182973.3:c.1152+104dup	NP_892018.1:n.1152+104dup
NM_001395513.1:c.1254+104dup MANE Select	NP_001382442.1:n.1254+104dup