Canonical Allele Identifier: CA1139798087

Gene: SELENOF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.86876787G= , CM000663.2:g.86876787G=	GRCh38
NC_000001.10:g.87342470G= , CM000663.1:g.87342470G=	GRCh37
NC_000001.9:g.87115058G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331835.10:c.316+3875C= MANE Select	ENSP00000328729.6:n.316+3875C=
ENST00000648872.1:c.316+3875C=	ENSP00000497584.1:n.316+3875C=
ENST00000331835.9:c.316+3875C=	ENSP00000328729.6:n.316+3875C=
ENST00000370554.5:c.316+3875C=	ENSP00000359585.2:n.316+3875C=
ENST00000401030.4:c.357+3875C=	ENSP00000383810.4:n.357+3875C=
ENST00000467557.1:c.492+3875C=
ENST00000469566.5:n.342+3875C=
ENST00000497861.5:c.177+3875C=	ENSP00000488294.1:n.177+3875C=
ENST00000611507.4:c.313+3875C=	ENSP00000481113.1:n.313+3875C=
ENST00000616787.4:c.313+3875C=	ENSP00000484190.1:n.313+3875C=
NM_004261.3:c.316+3875C=	NP_004252.2:n.316+3875C=
NM_203341.1:c.316+3875C=	NP_976086.1:n.316+3875C=
NM_004261.4:c.316+3875C=	NP_004252.2:n.316+3875C=
NM_203341.2:c.316+3875C=	NP_976086.1:n.316+3875C=
NR_144512.1:n.393+3875C=
NR_144513.1:n.377+3875C=
NM_004261.5:c.316+3875C= MANE Select	NP_004252.2:n.316+3875C=
NM_203341.3:c.316+3875C=	NP_976086.1:n.316+3875C=