Canonical Allele Identifier: CA1917818832
Community Standard Title: NM_012339.5(TSPAN15):c.357+305T=
Gene: TSPAN15 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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