Canonical Allele Identifier: CA2675401166
Gene: SMAD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136154203_136154208del , CM000667.2:g.136154203_136154208del GRCh38
NC_000005.9:g.135489892_135489897del , CM000667.1:g.135489892_135489897del GRCh37
NC_000005.8:g.135517791_135517796del NCBI36
NG_032037.1:g.26357_26362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000509297.6:c.403+40_403+45del ENSP00000426696.2:n.403+40_403+45del
ENST00000545279.6:c.403+40_403+45del MANE Select ENSP00000441954.2:n.403+40_403+45del
ENST00000514777.1:n.60-18231_60-18226del
ENST00000545279.5:c.403+40_403+45del ENSP00000441954.2:n.403+40_403+45del
ENST00000545620.5:c.403+40_403+45del ENSP00000446474.2:n.403+40_403+45del
NM_001001419.2:c.403+40_403+45del NP_001001419.1:n.403+40_403+45del
NM_001001420.2:c.403+40_403+45del NP_001001420.1:n.403+40_403+45del
NM_005903.6:c.403+40_403+45del NP_005894.3:n.403+40_403+45del
XR_948810.1:n.1973+1230_1973+1235del
XM_017009470.2:c.403+40_403+45del XP_016864959.1:n.403+40_403+45del
XM_024446046.1:c.403+40_403+45del XP_024301814.1:n.403+40_403+45del
XM_024446047.1:c.403+40_403+45del XP_024301815.1:n.403+40_403+45del
NM_005903.7:c.403+40_403+45del MANE Select NP_005894.3:n.403+40_403+45del
NM_001001419.3:c.403+40_403+45del NP_001001419.1:n.403+40_403+45del
NM_001001420.3:c.403+40_403+45del NP_001001420.1:n.403+40_403+45del