Canonical Allele Identifier: CA318130400

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1031431618
• COSMIC: COSN1254306 ; COSN5767433
• MyVariant Identifiers: chr21:g.19653598A>C (hg19) ; chr21:g.18281281A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281281A>C , CM000683.2:g.18281281A>C	GRCh38
NC_000021.8:g.19653598A>C , CM000683.1:g.19653598A>C	GRCh37
NC_000021.7:g.18575469A>C	NCBI36
NG_012207.1:g.127373T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2487-60T>G MANE Select	ENSP00000284885.3:n.2487-60T>G
ENST00000284885.7:c.2487-60T>G	ENSP00000284885.3:n.2487-60T>G
NM_002772.2:c.2487-60T>G	NP_002763.2:n.2487-60T>G
XM_011529654.1:c.2622-60T>G	XP_011527956.1:n.2622-60T>G
XM_011529655.1:c.2622-60T>G	XP_011527957.1:n.2622-60T>G
XM_011529656.1:c.2622-60T>G	XP_011527958.1:n.2622-60T>G
XM_011529657.1:c.2577-60T>G	XP_011527959.1:n.2577-60T>G
XM_011529658.1:c.2541-60T>G	XP_011527960.1:n.2541-60T>G
XM_011529659.1:c.2532-60T>G	XP_011527961.1:n.2532-60T>G
XM_011529654.2:c.2622-60T>G	XP_011527956.1:n.2622-60T>G
XM_011529656.2:c.2622-60T>G	XP_011527958.1:n.2622-60T>G
XM_011529657.2:c.2577-60T>G	XP_011527959.1:n.2577-60T>G
XM_011529658.2:c.2541-60T>G	XP_011527960.1:n.2541-60T>G
NM_002772.3:c.2487-60T>G MANE Select	NP_002763.3:n.2487-60T>G