Canonical Allele Identifier: CA2777663991

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788712_120788716del , CM000669.2:g.120788712_120788716del	GRCh38
NC_000007.13:g.120428766_120428770del , CM000669.1:g.120428766_120428770del	GRCh37
NC_000007.12:g.120216002_120216006del	NCBI36
NG_023203.1:g.74409_74413del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.795_799del MANE Select	ENSP00000222747.3:p.Asn265LysfsTer22
ENST00000222747.7:c.795_799del	ENSP00000222747.3:p.Asn265LysfsTer22
ENST00000415871.5:c.795_799del	ENSP00000397699.1:p.Asn265LysfsTer22
ENST00000450414.5:c.774_778del	ENSP00000397411.1:n.774_778del
NM_012338.3:c.795_799del	NP_036470.1:p.Asn265LysfsTer22
XM_005250239.1:c.795_799del	XP_005250296.1:p.Asn265LysfsTer22
XM_011515993.1:c.795_799del	XP_011514295.1:p.Asn265LysfsTer22
XM_011515994.1:c.795_799del	XP_011514296.1:p.Asn265LysfsTer22
XM_005250239.3:c.795_799del	XP_005250296.1:p.Asn265LysfsTer22
XM_017011913.1:c.720_724del	XP_016867402.1:p.Asn240LysfsTer22
NM_012338.4:c.795_799del MANE Select	NP_036470.1:p.Asn265LysfsTer22