Canonical Allele Identifier: CA409847823

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1316506067
• gnomAD v2: 21-19653356-C-T
• gnomAD v3: 21-18281039-C-T
• gnomAD v4: 21-18281039-C-T
• MyVariant Identifiers: chr21:g.19653356C>T (hg19) ; chr21:g.18281039C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281039C>T , CM000683.2:g.18281039C>T	GRCh38
NC_000021.8:g.19653356C>T , CM000683.1:g.19653356C>T	GRCh37
NC_000021.7:g.18575227C>T	NCBI36
NG_012207.1:g.127615G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2668+1G>A MANE Select	ENSP00000284885.3:n.2668+1G>A
ENST00000284885.7:c.2668+1G>A	ENSP00000284885.3:n.2668+1G>A
NM_002772.2:c.2668+1G>A	NP_002763.2:n.2668+1G>A
XM_011529654.1:c.2803+1G>A	XP_011527956.1:n.2803+1G>A
XM_011529655.1:c.2803+1G>A	XP_011527957.1:n.2803+1G>A
XM_011529656.1:c.2803+1G>A	XP_011527958.1:n.2803+1G>A
XM_011529657.1:c.2758+1G>A	XP_011527959.1:n.2758+1G>A
XM_011529658.1:c.2722+1G>A	XP_011527960.1:n.2722+1G>A
XM_011529659.1:c.2713+1G>A	XP_011527961.1:n.2713+1G>A
XM_011529654.2:c.2803+1G>A	XP_011527956.1:n.2803+1G>A
XM_011529656.2:c.2803+1G>A	XP_011527958.1:n.2803+1G>A
XM_011529657.2:c.2758+1G>A	XP_011527959.1:n.2758+1G>A
XM_011529658.2:c.2722+1G>A	XP_011527960.1:n.2722+1G>A
NM_002772.3:c.2668+1G>A MANE Select	NP_002763.3:n.2668+1G>A