Canonical Allele Identifier: CA2318296334

Gene: TMPRSS9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2410490T= , CM000681.2:g.2410490T=	GRCh38
NC_000019.9:g.2410488T= , CM000681.1:g.2410488T=	GRCh37
NC_000019.8:g.2361488T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696167.1:c.1254+96T= MANE Select	ENSP00000512457.1:n.1254+96T=
ENST00000648592.1:c.1254+96T=	ENSP00000498031.1:n.1254+96T=
ENST00000649857.1:c.1152+96T=	ENSP00000497651.1:n.1152+96T=
ENST00000332578.7:c.1152+96T=	ENSP00000330264.2:n.1152+96T=
ENST00000395264.3:n.1269+96T=
ENST00000613480.1:c.1152+96T=	ENSP00000482424.1:n.1152+96T=
NM_182973.1:c.1152+96T=	NP_892018.1:n.1152+96T=
XM_011527978.1:c.1254+96T=	XP_011526280.1:n.1254+96T=
XM_011527979.1:c.1155+96T=	XP_011526281.1:n.1155+96T=
XM_011527980.1:c.45+96T=	XP_011526282.1:n.45+96T=
XM_011527981.1:c.1254+96T=	XP_011526283.1:n.1254+96T=
XM_011527983.1:c.1254+96T=	XP_011526285.1:n.1254+96T=
NM_182973.2:c.1152+96T=	NP_892018.1:n.1152+96T=
XM_011527978.2:c.1254+96T=	XP_011526280.1:n.1254+96T=
NM_001385642.1:c.558+96T=	NP_001372571.1:n.558+96T=
NM_182973.3:c.1152+96T=	NP_892018.1:n.1152+96T=
NM_001395513.1:c.1254+96T= MANE Select	NP_001382442.1:n.1254+96T=