Canonical Allele Identifier: CA304223021

Gene: TMPRSS9

Linked Data

• dbSNP Id: rs948064639
• gnomAD v3: 19-2410502-G-A
• gnomAD v4: 19-2410502-G-A
• MyVariant Identifiers: chr19:g.2410500G>A (hg19) ; chr19:g.2410502G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2410502G>A , CM000681.2:g.2410502G>A	GRCh38
NC_000019.9:g.2410500G>A , CM000681.1:g.2410500G>A	GRCh37
NC_000019.8:g.2361500G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696167.1:c.1254+108G>A MANE Select	ENSP00000512457.1:n.1254+108G>A
ENST00000648592.1:c.1254+108G>A	ENSP00000498031.1:n.1254+108G>A
ENST00000649857.1:c.1152+108G>A	ENSP00000497651.1:n.1152+108G>A
ENST00000332578.7:c.1152+108G>A	ENSP00000330264.2:n.1152+108G>A
ENST00000395264.3:n.1269+108G>A
ENST00000613480.1:c.1152+108G>A	ENSP00000482424.1:n.1152+108G>A
NM_182973.1:c.1152+108G>A	NP_892018.1:n.1152+108G>A
XM_011527978.1:c.1254+108G>A	XP_011526280.1:n.1254+108G>A
XM_011527979.1:c.1155+108G>A	XP_011526281.1:n.1155+108G>A
XM_011527980.1:c.45+108G>A	XP_011526282.1:n.45+108G>A
XM_011527981.1:c.1254+108G>A	XP_011526283.1:n.1254+108G>A
XM_011527983.1:c.1254+108G>A	XP_011526285.1:n.1254+108G>A
NM_182973.2:c.1152+108G>A	NP_892018.1:n.1152+108G>A
XM_011527978.2:c.1254+108G>A	XP_011526280.1:n.1254+108G>A
NM_001385642.1:c.558+108G>A	NP_001372571.1:n.558+108G>A
NM_182973.3:c.1152+108G>A	NP_892018.1:n.1152+108G>A
NM_001395513.1:c.1254+108G>A MANE Select	NP_001382442.1:n.1254+108G>A