Canonical Allele Identifier: CA9066216

Gene: TMPRSS9

Linked Data

• ExAC: 19:2410392 GGTGAGCCCCCGATGCCCCAGACCCCAGAAAAACACAGAAATAGACACGAGCATGTTCAAATGCTGAGCAATTCACAGATATCTGGATGCCCGCT / G
• gnomAD v4: 19-2410394-GGTGAGCCCCCGATGCCCCAGACCCCAGAAAAACACAGAAATAGACACGAGCATGTTCAAATGCTGAGCAATTCACAGATATCTGGATGCCCGCT-G
• MyVariant Identifiers: chr19:g.2410393_2410486del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2410405_2410498del , CM000681.2:g.2410405_2410498del	GRCh38
NC_000019.9:g.2410403_2410496del , CM000681.1:g.2410403_2410496del	GRCh37
NC_000019.8:g.2361403_2361496del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696167.1:c.1254+11_1254+104del MANE Select	ENSP00000512457.1:n.1254+11_1254+104del
ENST00000648592.1:c.1254+11_1254+104del	ENSP00000498031.1:n.1254+11_1254+104del
ENST00000649857.1:c.1152+11_1152+104del	ENSP00000497651.1:n.1152+11_1152+104del
ENST00000332578.7:c.1152+11_1152+104del	ENSP00000330264.2:n.1152+11_1152+104del
ENST00000395264.3:n.1269+11_1269+104del
ENST00000613480.1:c.1152+11_1152+104del	ENSP00000482424.1:n.1152+11_1152+104del
NM_182973.1:c.1152+11_1152+104del	NP_892018.1:n.1152+11_1152+104del
XM_011527978.1:c.1254+11_1254+104del	XP_011526280.1:n.1254+11_1254+104del
XM_011527979.1:c.1155+11_1155+104del	XP_011526281.1:n.1155+11_1155+104del
XM_011527980.1:c.45+11_45+104del	XP_011526282.1:n.45+11_45+104del
XM_011527981.1:c.1254+11_1254+104del	XP_011526283.1:n.1254+11_1254+104del
XM_011527983.1:c.1254+11_1254+104del	XP_011526285.1:n.1254+11_1254+104del
NM_182973.2:c.1152+11_1152+104del	NP_892018.1:n.1152+11_1152+104del
XM_011527978.2:c.1254+11_1254+104del	XP_011526280.1:n.1254+11_1254+104del
NM_001385642.1:c.558+11_558+104del	NP_001372571.1:n.558+11_558+104del
NM_182973.3:c.1152+11_1152+104del	NP_892018.1:n.1152+11_1152+104del
NM_001395513.1:c.1254+11_1254+104del MANE Select	NP_001382442.1:n.1254+11_1254+104del