Canonical Allele Identifier: CA117819193

Gene: SELENOP

Linked Data

• dbSNP Id: rs538938617
• gnomAD v3: 5-42804056-C-T
• gnomAD v4: 5-42804056-C-T
• MyVariant Identifiers: chr5:g.42804158C>T (hg19) ; chr5:g.42804056C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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