Canonical Allele Identifier: CA1948071409

Gene: C11orf21 TSPAN32

Linked Data

• dbSNP Id: rs1847746412

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2301507_2301508del , CM000673.2:g.2301507_2301508del	GRCh38
NC_000011.9:g.2322737_2322738del , CM000673.1:g.2322737_2322738del	GRCh37
NC_000011.8:g.2279313_2279314del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381153.8:c.53+251_53+252del (C11orf21) MANE Select	ENSP00000370545.4:n.53+251_53+252del
ENST00000381153.7:c.53+251_53+252del (C11orf21)	ENSP00000370545.3:n.53+251_53+252del
ENST00000456145.2:c.106+251_106+252del (C11orf21)	ENSP00000406541.2:n.106+251_106+252del
ENST00000470369.1:n.368_369del (C11orf21)
ENST00000495467.1:n.168+1377_168+1378del (C11orf21)
NM_001142946.1:c.106+251_106+252del (C11orf21)	NP_001136418.1:n.106+251_106+252del
NR_024621.1:n.158+251_158+252del (C11orf21)
XM_011520034.1:c.106+251_106+252del (C11orf21)	XP_011518336.1:n.106+251_106+252del
NM_001142946.2:c.106+251_106+252del (C11orf21)	NP_001136418.1:n.106+251_106+252del
NM_001329958.1:c.53+251_53+252del (C11orf21)	NP_001316887.1:n.53+251_53+252del
NR_138249.1:n.168+1377_168+1378del (C11orf21)
XM_011520034.2:c.106+251_106+252del (C11orf21)	XP_011518336.1:n.106+251_106+252del
XM_017017067.1:c.-24-1337_-24-1336del (TSPAN32)	XP_016872556.1:n.-24-1337_-24-1336del
NM_001142946.3:c.106+251_106+252del (C11orf21)	NP_001136418.1:n.106+251_106+252del
NM_001329958.2:c.53+251_53+252del (C11orf21) MANE Select	NP_001316887.1:n.53+251_53+252del
NR_138249.2:n.259+1377_259+1378del (C11orf21)