Canonical Allele Identifier: CA13268815
Gene: TSPAN15 HGNC NCBI

Linked Data

dbSNP Id: rs78707713

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69485520T>C , CM000672.2:g.69485520T>C GRCh38
NC_000010.10:g.71245276T>C , CM000672.1:g.71245276T>C GRCh37
NC_000010.9:g.70915282T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000373290.7:c.357+305T>C MANE Select ENSP00000362387.2:p.=
ENST00000373290.6:c.357+305T>C ENSP00000362387.2:p.=
ENST00000452130.1:n.84+305T>C ENSP00000404528.1:p.=
ENST00000475069.5:n.127+305T>C
NM_012339.3:c.357+305T>C NP_036471.1:p.=
XM_005269667.3:c.97-10074T>C XP_005269724.1:p.=
XM_006717738.2:c.285+305T>C XP_006717801.1:p.=
XR_945642.1:n.487+305T>C
NM_001351263.1:c.97-10074T>C NP_001338192.1:p.=
NM_012339.4:c.357+305T>C NP_036471.1:p.=
NR_147091.1:n.485+305T>C
XM_017016010.1:c.357+305T>C XP_016871499.1:p.=
XR_001747072.1:n.488+305T>C
XR_001747073.1:n.488+305T>C
XR_001747074.1:n.485+305T>C
NM_012339.5:c.357+305T>C MANE Select NP_036471.1:p.=
NM_001351263.2:c.97-10074T>C NP_001338192.1:p.=
NR_147091.2:n.487+305T>C