Canonical Allele Identifier: CA1683032389
Gene: MAD1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2225428G= , CM000669.2:g.2225428G= GRCh38
NC_000007.13:g.2265063G= , CM000669.1:g.2265063G= GRCh37
NC_000007.12:g.2231589G= NCBI36
NG_011518.1:g.12521C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265854.12:c.273C= MANE Select ENSP00000265854.7:p.Thr91=
ENST00000651235.1:c.*2681C= ENSP00000498895.1:n.*2681C=
ENST00000265854.11:c.273C= ENSP00000265854.7:p.Thr91=
ENST00000399654.6:c.273C= ENSP00000382562.2:p.Thr91=
ENST00000402746.5:c.-124-2674C= ENSP00000384155.1:n.-124-2674C=
ENST00000406869.5:c.273C= ENSP00000385334.1:p.Thr91=
ENST00000429625.5:c.60C= ENSP00000413139.1:p.Thr20=
ENST00000429779.1:c.273C= ENSP00000395457.1:p.Thr91=
ENST00000455998.5:c.151-2674C= ENSP00000390099.1:n.151-2674C=
NM_001013836.1:c.273C= NP_001013858.1:p.Thr91=
NM_001013837.1:c.273C= NP_001013859.1:p.Thr91=
NM_001304523.1:c.273C= NP_001291452.1:p.Thr91=
NM_001304524.1:c.-124-2674C= NP_001291453.1:n.-124-2674C=
NM_003550.2:c.273C= NP_003541.2:p.Thr91=
XM_005249877.1:c.151-2674C= XP_005249934.1:n.151-2674C=
XM_011515567.1:c.273C= XP_011513869.1:p.Thr91=
XM_011515568.1:c.273C= XP_011513870.1:p.Thr91=
XM_011515570.1:c.273C= XP_011513872.1:p.Thr91=
XM_011515568.3:c.273C= XP_011513870.1:p.Thr91=
XM_017012690.1:c.465C= XP_016868179.1:p.Thr155=
XM_024446951.1:c.273C= XP_024302719.1:p.Thr91=
XM_024446952.1:c.273C= XP_024302720.1:p.Thr91=
NM_001013836.2:c.273C= MANE Select NP_001013858.1:p.Thr91=
NM_001013837.2:c.273C= NP_001013859.1:p.Thr91=
NM_001304523.2:c.273C= NP_001291452.1:p.Thr91=
NM_001304524.2:c.-124-2674C= NP_001291453.1:n.-124-2674C=
NM_003550.3:c.273C= NP_003541.2:p.Thr91=