Canonical Allele Identifier: CA10732101
Gene: SELENOF HGNC NCBI

Linked Data

dbSNP Id: rs1407131
gnomAD v2: 1-87378627-T-C
gnomAD v3: 1-86912944-T-C
gnomAD v4: 1-86912944-T-C

Genomic Alleles

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

Transcript Alleles

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