Canonical Allele Identifier: CA1542332966
Gene: SELENOP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.42804056C= , CM000667.2:g.42804056C= GRCh38
NC_000005.9:g.42804158C= , CM000667.1:g.42804158C= GRCh37
NC_000005.8:g.42839915C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000514985.6:c.534+600G= MANE Select ENSP00000420939.1:n.534+600G=
ENST00000506577.5:c.534+600G= ENSP00000425915.1:n.534+600G=
ENST00000507920.5:c.204-2725G= ENSP00000473340.1:n.204-2725G=
ENST00000509276.5:n.334+600G=
ENST00000510965.1:c.534+600G= ENSP00000427414.1:n.534+600G=
ENST00000511224.5:c.534+600G= ENSP00000427671.1:n.534+600G=
ENST00000512980.5:n.2726+600G=
ENST00000513303.5:n.488-2725G=
ENST00000514218.5:c.534+600G= ENSP00000421626.1:n.534+600G=
ENST00000514403.1:n.521+600G=
ENST00000514985.5:c.534+600G= ENSP00000420939.1:n.534+600G=
NM_001085486.1:c.534+600G= NP_001078955.1:n.534+600G=
NM_001093726.1:c.624+600G= NP_001087195.1:n.624+600G=
NM_005410.2:c.534+600G= NP_005401.3:n.534+600G=
NM_001085486.2:c.534+600G= NP_001078955.1:n.534+600G=
NM_001093726.2:c.624+600G= NP_001087195.1:n.624+600G=
NM_005410.3:c.534+600G= NP_005401.3:n.534+600G=
NM_005410.4:c.534+600G= MANE Select NP_005401.3:n.534+600G=
NM_001085486.3:c.534+600G= NP_001078955.1:n.534+600G=
NM_001093726.3:c.624+600G= NP_001087195.1:n.624+600G=