Canonical Allele Identifier: CA2244611717
Gene: C17orf107 HGNC NCBI
CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4900744_4900768delinsGCCCCCACCCTTCACACTGGCCACA , CM000679.2:g.4900744_4900768delinsGCCCCCACCCTTCACACTGGCCACA GRCh38
NC_000017.10:g.4804039_4804063delinsGCCCCCACCCTTCACACTGGCCACA , CM000679.1:g.4804039_4804063delinsGCCCCCACCCTTCACACTGGCCACA GRCh37
NC_000017.9:g.4744818_4744842delinsGCCCCCACCCTTCACACTGGCCACA NCBI36
NG_008029.2:g.7308_7332delinsTGTGGCCAGTGTGAAGGGTGGGGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000381365.4:c.*211_*235delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) MANE Select ENSP00000370770.3:n.*211_*235delinsGCCCCC...
ENST00000649488.2:c.917+25_917+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) MANE Select ENSP00000497829.1:n.917+25_917+49delinsTG...
ENST00000649830.1:c.-17+25_-17+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) ENSP00000496907.1:n.-17+25_-17+49delinsTG...
ENST00000293780.4:c.917+25_917+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) ENSP00000293780.4:n.917+25_917+49delinsTG...
ENST00000381365.3:c.*211_*235delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) ENSP00000370770.3:n.*211_*235delinsGCCCCC...
ENST00000521575.1:c.*578_*602delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) ENSP00000429241.1:n.*578_*602delinsGCCCCC...
ENST00000572438.1:n.603+25_603+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE)
NM_000080.3:c.917+25_917+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) NP_000071.1:n.917+25_917+49delinsTGTGGCCA...
NM_001145536.1:c.*211_*235delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) NP_001139008.1:n.*211_*235delinsGCCCCCACC...
XM_011523612.1:c.546+238_546+262delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) XP_011521914.1:n.546+238_546+262delinsGCC...
XM_011523631.1:c.802+222_802+246delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) XP_011521933.1:n.802+222_802+246delinsTGT...
NM_000080.4:c.917+25_917+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) MANE Select NP_000071.1:n.917+25_917+49delinsTGTGGCCA...
XM_017024115.1:c.881+25_881+49delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE) XP_016879604.1:n.881+25_881+49delinsTGTGG...
XR_001752421.1:n.1647+222_1647+246delinsTGTGGCCAGTGTGAAGGGTGGGGGC (CHRNE)
NM_001145536.2:c.*211_*235delinsGCCCCCACCCTTCACACTGGCCACA (C17orf107) MANE Select NP_001139008.1:n.*211_*235delinsGCCCCCACC...