Canonical Allele Identifier: CA2579001717

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788683_120788685del , CM000669.2:g.120788683_120788685del	GRCh38
NC_000007.13:g.120428737_120428739del , CM000669.1:g.120428737_120428739del	GRCh37
NC_000007.12:g.120215973_120215975del	NCBI36
NG_023203.1:g.74441_74443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.827_829del MANE Select	ENSP00000222747.3:p.Val276del
ENST00000222747.7:c.827_829del	ENSP00000222747.3:p.Val276del
ENST00000415871.5:c.827_829del	ENSP00000397699.1:p.Val276del
ENST00000450414.5:c.806_808del	ENSP00000397411.1:n.806_808del
NM_012338.3:c.827_829del	NP_036470.1:p.Val276del
XM_005250239.1:c.827_829del	XP_005250296.1:p.Val276del
XM_011515993.1:c.827_829del	XP_011514295.1:p.Val276del
XM_011515994.1:c.827_829del	XP_011514296.1:p.Val276del
XM_005250239.3:c.827_829del	XP_005250296.1:p.Val276del
XM_017011913.1:c.752_754del	XP_016867402.1:p.Val251del
NM_012338.4:c.827_829del MANE Select	NP_036470.1:p.Val276del