Canonical Allele Identifier: CA1020838291

Gene: TMPRSS15

Linked Data

• gnomAD v3: 21-18280766-CTATT-C
• gnomAD v4: 21-18280766-CTATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280770_18280773del , CM000683.2:g.18280770_18280773del	GRCh38
NC_000021.8:g.19653087_19653090del , CM000683.1:g.19653087_19653090del	GRCh37
NC_000021.7:g.18574958_18574961del	NCBI36
NG_012207.1:g.127884_127887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+270_2668+273del MANE Select	ENSP00000284885.3:n.2668+270_2668+273del
ENST00000284885.7:c.2668+270_2668+273del	ENSP00000284885.3:n.2668+270_2668+273del
NM_002772.2:c.2668+270_2668+273del	NP_002763.2:n.2668+270_2668+273del
XM_011529654.1:c.2803+270_2803+273del	XP_011527956.1:n.2803+270_2803+273del
XM_011529655.1:c.2803+270_2803+273del	XP_011527957.1:n.2803+270_2803+273del
XM_011529656.1:c.2803+270_2803+273del	XP_011527958.1:n.2803+270_2803+273del
XM_011529657.1:c.2758+270_2758+273del	XP_011527959.1:n.2758+270_2758+273del
XM_011529658.1:c.2722+270_2722+273del	XP_011527960.1:n.2722+270_2722+273del
XM_011529659.1:c.2713+270_2713+273del	XP_011527961.1:n.2713+270_2713+273del
XM_011529654.2:c.2803+270_2803+273del	XP_011527956.1:n.2803+270_2803+273del
XM_011529656.2:c.2803+270_2803+273del	XP_011527958.1:n.2803+270_2803+273del
XM_011529657.2:c.2758+270_2758+273del	XP_011527959.1:n.2758+270_2758+273del
XM_011529658.2:c.2722+270_2722+273del	XP_011527960.1:n.2722+270_2722+273del
NM_002772.3:c.2668+270_2668+273del MANE Select	NP_002763.3:n.2668+270_2668+273del