Canonical Allele Identifier: CA2675401225
Gene: SMAD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136154247del , CM000667.2:g.136154247del GRCh38
NC_000005.9:g.135489936del , CM000667.1:g.135489936del GRCh37
NC_000005.8:g.135517835del NCBI36
NG_032037.1:g.26401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000509297.6:c.403+84del ENSP00000426696.2:n.403+84del
ENST00000545279.6:c.403+84del MANE Select ENSP00000441954.2:n.403+84del
ENST00000514777.1:n.60-18187del
ENST00000545279.5:c.403+84del ENSP00000441954.2:n.403+84del
ENST00000545620.5:c.403+84del ENSP00000446474.2:n.403+84del
NM_001001419.2:c.403+84del NP_001001419.1:n.403+84del
NM_001001420.2:c.403+84del NP_001001420.1:n.403+84del
NM_005903.6:c.403+84del NP_005894.3:n.403+84del
XR_948810.1:n.1973+1180del
XM_017009470.2:c.403+84del XP_016864959.1:n.403+84del
XM_024446046.1:c.403+84del XP_024301814.1:n.403+84del
XM_024446047.1:c.403+84del XP_024301815.1:n.403+84del
NM_005903.7:c.403+84del MANE Select NP_005894.3:n.403+84del
NM_001001419.3:c.403+84del NP_001001419.1:n.403+84del
NM_001001420.3:c.403+84del NP_001001420.1:n.403+84del