Canonical Allele Identifier: CA2635248300
Gene: PRPF8 HGNC NCBI

Linked Data

gnomAD v4: 17-1650750-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1650750G>C , CM000679.2:g.1650750G>C GRCh38
NC_000017.10:g.1554044G>C , CM000679.1:g.1554044G>C GRCh37
NC_000017.9:g.1500794G>C NCBI36
NG_009118.1:g.39133C>G
NG_033061.1:g.4349C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000573725.2:c.*52C>G ENSP00000460849.2:n.*52C>G
ENST00000703537.1:c.2808C>G
ENST00000703538.1:c.*6783C>G ENSP00000515361.1:n.*6783C>G
ENST00000703539.1:n.3374C>G
ENST00000703540.1:c.*52C>G ENSP00000515362.1:n.*52C>G
ENST00000304992.11:c.*52C>G MANE Select ENSP00000304350.6:n.*52C>G
ENST00000304992.10:c.*52C>G ENSP00000304350.6:n.*52C>G
ENST00000571958.1:c.259C>G
ENST00000572621.5:c.*52C>G ENSP00000460348.1:n.*52C>G
NM_006445.3:c.*52C>G NP_006436.3:n.*52C>G
XM_024450537.1:c.*52C>G XP_024306305.1:n.*52C>G
NM_006445.4:c.*52C>G MANE Select NP_006436.3:n.*52C>G