Canonical Allele Identifier: CA15104303
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs11209002
gnomAD v2: 1-67590461-T-C
gnomAD v3: 1-67124778-T-C
gnomAD v4: 1-67124778-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67124778T>C , CM000663.2:g.67124778T>C GRCh38
NC_000001.10:g.67590461T>C , CM000663.1:g.67590461T>C GRCh37
NC_000001.9:g.67363049T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000684719.1:c.233+974A>G MANE Select ENSP00000507487.1:n.233+974A>G
ENST00000371004.6:n.377+974A>G
ENST00000371006.5:c.233+974A>G ENSP00000360045.1:n.233+974A>G
ENST00000371007.6:c.233+974A>G ENSP00000360046.1:n.233+974A>G
ENST00000448166.6:c.233+974A>G ENSP00000415519.2:n.233+974A>G
ENST00000475209.6:c.233+974A>G ENSP00000432856.2:n.233+974A>G
ENST00000544837.5:c.233+974A>G ENSP00000444018.2:n.233+974A>G
ENST00000603691.1:c.233+974A>G ENSP00000474902.1:n.233+974A>G
ENST00000621590.4:c.233+974A>G ENSP00000481294.1:n.233+974A>G
NM_001276351.1:c.233+974A>G NP_001263280.1:n.233+974A>G
NM_001276352.1:c.233+974A>G NP_001263281.1:n.233+974A>G
NR_075077.1:n.378+974A>G
XM_011541464.1:c.233+974A>G XP_011539766.1:n.233+974A>G
XM_011541465.1:c.233+974A>G XP_011539767.1:n.233+974A>G
XM_011541466.1:c.233+974A>G XP_011539768.1:n.233+974A>G
XM_011541467.1:c.233+974A>G XP_011539769.1:n.233+974A>G
XM_011541471.1:c.233+974A>G XP_011539773.1:n.233+974A>G
XM_011541472.1:c.233+974A>G XP_011539774.1:n.233+974A>G
XM_011541473.1:c.233+974A>G XP_011539775.1:n.233+974A>G
XM_011541474.1:c.233+974A>G XP_011539776.1:n.233+974A>G
XM_011541475.1:c.233+974A>G XP_011539777.1:n.233+974A>G
XM_011541465.2:c.233+974A>G XP_011539767.1:n.233+974A>G
XM_011541466.2:c.233+974A>G XP_011539768.1:n.233+974A>G
XM_011541473.2:c.233+974A>G XP_011539775.1:n.233+974A>G
XM_017001276.1:c.233+974A>G XP_016856765.1:n.233+974A>G
XM_017001277.1:c.233+974A>G XP_016856766.1:n.233+974A>G
NM_001276351.2:c.233+974A>G MANE Select NP_001263280.1:n.233+974A>G
NM_001276352.2:c.233+974A>G NP_001263281.1:n.233+974A>G
NR_075077.2:n.377+974A>G