Canonical Allele Identifier: CA1020838335

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2074690521
• gnomAD v3: 21-18280968-GATA-G
• gnomAD v4: 21-18280968-GATA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280972_18280974del , CM000683.2:g.18280972_18280974del	GRCh38
NC_000021.8:g.19653289_19653291del , CM000683.1:g.19653289_19653291del	GRCh37
NC_000021.7:g.18575160_18575162del	NCBI36
NG_012207.1:g.127683_127685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+69_2668+71del MANE Select	ENSP00000284885.3:n.2668+69_2668+71del
ENST00000284885.7:c.2668+69_2668+71del	ENSP00000284885.3:n.2668+69_2668+71del
NM_002772.2:c.2668+69_2668+71del	NP_002763.2:n.2668+69_2668+71del
XM_011529654.1:c.2803+69_2803+71del	XP_011527956.1:n.2803+69_2803+71del
XM_011529655.1:c.2803+69_2803+71del	XP_011527957.1:n.2803+69_2803+71del
XM_011529656.1:c.2803+69_2803+71del	XP_011527958.1:n.2803+69_2803+71del
XM_011529657.1:c.2758+69_2758+71del	XP_011527959.1:n.2758+69_2758+71del
XM_011529658.1:c.2722+69_2722+71del	XP_011527960.1:n.2722+69_2722+71del
XM_011529659.1:c.2713+69_2713+71del	XP_011527961.1:n.2713+69_2713+71del
XM_011529654.2:c.2803+69_2803+71del	XP_011527956.1:n.2803+69_2803+71del
XM_011529656.2:c.2803+69_2803+71del	XP_011527958.1:n.2803+69_2803+71del
XM_011529657.2:c.2758+69_2758+71del	XP_011527959.1:n.2758+69_2758+71del
XM_011529658.2:c.2722+69_2722+71del	XP_011527960.1:n.2722+69_2722+71del
NM_002772.3:c.2668+69_2668+71del MANE Select	NP_002763.3:n.2668+69_2668+71del