Canonical Allele Identifier: CA2580590444

Gene: SELENOP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42804013T>A , CM000667.2:g.42804013T>A	GRCh38
NC_000005.9:g.42804115T>A , CM000667.1:g.42804115T>A	GRCh37
NC_000005.8:g.42839872T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000514985.6:c.534+643A>T MANE Select	ENSP00000420939.1:n.534+643A>T
ENST00000506577.5:c.534+643A>T	ENSP00000425915.1:n.534+643A>T
ENST00000507920.5:c.204-2682A>T	ENSP00000473340.1:n.204-2682A>T
ENST00000509276.5:n.334+643A>T
ENST00000510965.1:c.534+643A>T	ENSP00000427414.1:n.534+643A>T
ENST00000511224.5:c.534+643A>T	ENSP00000427671.1:n.534+643A>T
ENST00000512980.5:n.2726+643A>T
ENST00000513303.5:n.488-2682A>T
ENST00000514218.5:c.534+643A>T	ENSP00000421626.1:n.534+643A>T
ENST00000514403.1:n.521+643A>T
ENST00000514985.5:c.534+643A>T	ENSP00000420939.1:n.534+643A>T
NM_001085486.1:c.534+643A>T	NP_001078955.1:n.534+643A>T
NM_001093726.1:c.624+643A>T	NP_001087195.1:n.624+643A>T
NM_005410.2:c.534+643A>T	NP_005401.3:n.534+643A>T
NM_001085486.2:c.534+643A>T	NP_001078955.1:n.534+643A>T
NM_001093726.2:c.624+643A>T	NP_001087195.1:n.624+643A>T
NM_005410.3:c.534+643A>T	NP_005401.3:n.534+643A>T
NM_005410.4:c.534+643A>T MANE Select	NP_005401.3:n.534+643A>T
NM_001085486.3:c.534+643A>T	NP_001078955.1:n.534+643A>T
NM_001093726.3:c.624+643A>T	NP_001087195.1:n.624+643A>T