Canonical Allele Identifier: CA13406348

Gene: C11orf21 TSPAN32

Linked Data

• dbSNP Id: rs11022157
• gnomAD v2: 11-2322829-C-A
• gnomAD v3: 11-2301599-C-A
• gnomAD v4: 11-2301599-C-A
• MyVariant Identifiers: chr11:g.2322829C>A (hg19) ; chr11:g.2301599C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2301599C>A , CM000673.2:g.2301599C>A	GRCh38
NC_000011.9:g.2322829C>A , CM000673.1:g.2322829C>A	GRCh37
NC_000011.8:g.2279405C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381153.8:c.53+157G>T (C11orf21) MANE Select	ENSP00000370545.4:n.53+157G>T
ENST00000381153.7:c.53+157G>T (C11orf21)	ENSP00000370545.3:n.53+157G>T
ENST00000456145.2:c.106+157G>T (C11orf21)	ENSP00000406541.2:n.106+157G>T
ENST00000470369.1:n.274G>T (C11orf21)
ENST00000495467.1:n.168+1283G>T (C11orf21)
NM_001142946.1:c.106+157G>T (C11orf21)	NP_001136418.1:n.106+157G>T
NR_024621.1:n.158+157G>T (C11orf21)
XM_011520034.1:c.106+157G>T (C11orf21)	XP_011518336.1:n.106+157G>T
NM_001142946.2:c.106+157G>T (C11orf21)	NP_001136418.1:n.106+157G>T
NM_001329958.1:c.53+157G>T (C11orf21)	NP_001316887.1:n.53+157G>T
NR_138249.1:n.168+1283G>T (C11orf21)
XM_011520034.2:c.106+157G>T (C11orf21)	XP_011518336.1:n.106+157G>T
XM_017017067.1:c.-24-1245C>A (TSPAN32)	XP_016872556.1:n.-24-1245C>A
NM_001142946.3:c.106+157G>T (C11orf21)	NP_001136418.1:n.106+157G>T
NM_001329958.2:c.53+157G>T (C11orf21) MANE Select	NP_001316887.1:n.53+157G>T
NR_138249.2:n.259+1283G>T (C11orf21)