Canonical Allele Identifier: CA1139870944

Gene: SELENOF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.86912944T= , CM000663.2:g.86912944T=	GRCh38
NC_000001.10:g.87378627T= , CM000663.1:g.87378627T=	GRCh37
NC_000001.9:g.87151215T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331835.10:c.84+1084A= MANE Select	ENSP00000328729.6:n.84+1084A=
ENST00000648872.1:c.84+1084A=	ENSP00000497584.1:n.84+1084A=
ENST00000331835.9:c.84+1084A=	ENSP00000328729.6:n.84+1084A=
ENST00000370554.5:c.84+1084A=	ENSP00000359585.2:n.84+1084A=
ENST00000401030.4:c.84+1084A=	ENSP00000383810.4:n.84+1084A=
ENST00000467557.1:c.260+862A=
ENST00000469566.5:n.110+1371A=
ENST00000611507.4:c.84+1084A=	ENSP00000481113.1:n.84+1084A=
ENST00000616787.4:c.84+1084A=	ENSP00000484190.1:n.84+1084A=
NM_004261.3:c.84+1084A=	NP_004252.2:n.84+1084A=
NM_203341.1:c.84+1084A=	NP_976086.1:n.84+1084A=
NM_004261.4:c.84+1084A=	NP_004252.2:n.84+1084A=
NM_203341.2:c.84+1084A=	NP_976086.1:n.84+1084A=
NR_144512.1:n.161+1371A=
NR_144513.1:n.145+1489A=
NM_004261.5:c.84+1084A= MANE Select	NP_004252.2:n.84+1084A=
NM_203341.3:c.84+1084A=	NP_976086.1:n.84+1084A=