Canonical Allele Identifier: CA16042682
Gene: TSPAN12 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 373552
ClinVar RCV Id: RCV000413300
dbSNP Id: rs1057518477

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120840111T>C , CM000669.2:g.120840111T>C GRCh38
NC_000007.12:g.120267401T>C NCBI36
NC_000007.13:g.120480165T>C , CM000669.1:g.120480165T>C GRCh37
NG_023203.1:g.23013A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222747.7:c.67-2A>G ENSP00000222747.3:p.=
ENST00000415871.5:c.67-2A>G ENSP00000397699.1:p.=
ENST00000424710.5:c.67-2A>G ENSP00000404942.1:p.=
ENST00000430985.1:c.67-2A>G ENSP00000388819.1:p.=
ENST00000433758.5:c.67-2A>G ENSP00000399059.1:p.=
ENST00000441017.5:c.67-2A>G ENSP00000411158.1:p.=
NM_012338.3:c.67-2A>G VV NP_036470.1:p.=
XM_005250239.1:c.67-2A>G XP_005250296.1:p.=
XM_011515993.1:c.67-2A>G XP_011514295.1:p.=
XM_011515994.1:c.67-2A>G XP_011514296.1:p.=