Canonical Allele Identifier: CA2581672710

Gene: C1orf141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67131436G>T , CM000663.2:g.67131436G>T	GRCh38
NC_000001.10:g.67597119G>T , CM000663.1:g.67597119G>T	GRCh37
NC_000001.9:g.67369707G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001276351.2:c.-103-209C>A MANE Select	NP_001263280.1:n.-103-209C>A
ENST00000684719.1:c.-103-209C>A MANE Select	ENSP00000507487.1:n.-103-209C>A
NM_001276351.1:c.-103-209C>A	NP_001263280.1:n.-103-209C>A
NM_001276352.1:c.-103-209C>A	NP_001263281.1:n.-103-209C>A
NM_001276352.2:c.-103-209C>A	NP_001263281.1:n.-103-209C>A
NR_075077.1:n.43-209C>A
NR_075077.2:n.42-209C>A
ENST00000371004.6:n.42-209C>A
ENST00000371007.6:c.-103-209C>A	ENSP00000360046.1:n.-103-209C>A
ENST00000448166.6:c.-103-209C>A	ENSP00000415519.2:n.-103-209C>A
ENST00000544837.5:c.-103-209C>A	ENSP00000444018.2:n.-103-209C>A
ENST00000603691.1:c.-103-209C>A	ENSP00000474902.1:n.-103-209C>A
XM_011541464.1:c.-103-209C>A	XP_011539766.1:n.-103-209C>A
XM_011541465.1:c.-18+3494C>A	XP_011539767.1:n.-18+3494C>A
XM_011541465.2:c.-18+3494C>A	XP_011539767.1:n.-18+3494C>A
XM_011541466.1:c.-17-4179C>A	XP_011539768.1:n.-17-4179C>A
XM_011541466.2:c.-17-4179C>A	XP_011539768.1:n.-17-4179C>A
XM_011541471.1:c.-103-209C>A	XP_011539773.1:n.-103-209C>A