Canonical Allele Identifier: CA9984016

Gene: TMPRSS15

Linked Data

• ClinVar Variation Id: 2798763
• ClinVar RCV Id: RCV003675978
• dbSNP Id: rs779184545
• ExAC: 21:19653550 A / G
• gnomAD v2: 21-19653550-A-G
• gnomAD v3: 21-18281233-A-G
• gnomAD v4: 21-18281233-A-G
• MyVariant Identifiers: chr21:g.19653550A>G (hg19) ; chr21:g.18281233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281233A>G , CM000683.2:g.18281233A>G	GRCh38
NC_000021.8:g.19653550A>G , CM000683.1:g.19653550A>G	GRCh37
NC_000021.7:g.18575421A>G	NCBI36
NG_012207.1:g.127421T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2487-12T>C MANE Select	ENSP00000284885.3:n.2487-12T>C
ENST00000284885.7:c.2487-12T>C	ENSP00000284885.3:n.2487-12T>C
NM_002772.2:c.2487-12T>C	NP_002763.2:n.2487-12T>C
XM_011529654.1:c.2622-12T>C	XP_011527956.1:n.2622-12T>C
XM_011529655.1:c.2622-12T>C	XP_011527957.1:n.2622-12T>C
XM_011529656.1:c.2622-12T>C	XP_011527958.1:n.2622-12T>C
XM_011529657.1:c.2577-12T>C	XP_011527959.1:n.2577-12T>C
XM_011529658.1:c.2541-12T>C	XP_011527960.1:n.2541-12T>C
XM_011529659.1:c.2532-12T>C	XP_011527961.1:n.2532-12T>C
XM_011529654.2:c.2622-12T>C	XP_011527956.1:n.2622-12T>C
XM_011529656.2:c.2622-12T>C	XP_011527958.1:n.2622-12T>C
XM_011529657.2:c.2577-12T>C	XP_011527959.1:n.2577-12T>C
XM_011529658.2:c.2541-12T>C	XP_011527960.1:n.2541-12T>C
NM_002772.3:c.2487-12T>C MANE Select	NP_002763.3:n.2487-12T>C