Canonical Allele Identifier: CA558841130

Gene: SELENOP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42805863C>G , CM000667.2:g.42805863C>G	GRCh38
NC_000005.9:g.42805965C>G , CM000667.1:g.42805965C>G	GRCh37
NC_000005.8:g.42841722C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000514985.6:c.416+1033G>C MANE Select	ENSP00000420939.1:n.416+1033G>C
ENST00000505309.1:n.468+1033G>C
ENST00000506577.5:c.416+1033G>C	ENSP00000425915.1:n.416+1033G>C
ENST00000507920.5:c.203+2288G>C	ENSP00000473340.1:n.203+2288G>C
ENST00000509276.5:n.217-1090G>C
ENST00000510965.1:c.416+1033G>C	ENSP00000427414.1:n.416+1033G>C
ENST00000511224.5:c.416+1033G>C	ENSP00000427671.1:n.416+1033G>C
ENST00000512980.5:n.1519G>C
ENST00000513303.5:n.487+1033G>C
ENST00000514218.5:c.416+1033G>C	ENSP00000421626.1:n.416+1033G>C
ENST00000514403.1:n.403+1033G>C
ENST00000514985.5:c.416+1033G>C	ENSP00000420939.1:n.416+1033G>C
NM_001085486.1:c.416+1033G>C	NP_001078955.1:n.416+1033G>C
NM_001093726.1:c.506+1033G>C	NP_001087195.1:n.506+1033G>C
NM_005410.2:c.416+1033G>C	NP_005401.3:n.416+1033G>C
NM_001085486.2:c.416+1033G>C	NP_001078955.1:n.416+1033G>C
NM_001093726.2:c.506+1033G>C	NP_001087195.1:n.506+1033G>C
NM_005410.3:c.416+1033G>C	NP_005401.3:n.416+1033G>C
NM_005410.4:c.416+1033G>C MANE Select	NP_005401.3:n.416+1033G>C
NM_001085486.3:c.416+1033G>C	NP_001078955.1:n.416+1033G>C
NM_001093726.3:c.506+1033G>C	NP_001087195.1:n.506+1033G>C