Canonical Allele Identifier: CA2675401230

Gene: SMAD5

Linked Data

• gnomAD v4: 5-136154253-GGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136154256_136154258del , CM000667.2:g.136154256_136154258del	GRCh38
NC_000005.9:g.135489945_135489947del , CM000667.1:g.135489945_135489947del	GRCh37
NC_000005.8:g.135517844_135517846del	NCBI36
NG_032037.1:g.26410_26412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509297.6:c.403+93_403+95del	ENSP00000426696.2:n.403+93_403+95del
ENST00000545279.6:c.403+93_403+95del MANE Select	ENSP00000441954.2:n.403+93_403+95del
ENST00000514777.1:n.60-18178_60-18176del
ENST00000545279.5:c.403+93_403+95del	ENSP00000441954.2:n.403+93_403+95del
ENST00000545620.5:c.403+93_403+95del	ENSP00000446474.2:n.403+93_403+95del
NM_001001419.2:c.403+93_403+95del	NP_001001419.1:n.403+93_403+95del
NM_001001420.2:c.403+93_403+95del	NP_001001420.1:n.403+93_403+95del
NM_005903.6:c.403+93_403+95del	NP_005894.3:n.403+93_403+95del
XR_948810.1:n.1973+1171_1973+1173del
XM_017009470.2:c.403+93_403+95del	XP_016864959.1:n.403+93_403+95del
XM_024446046.1:c.403+93_403+95del	XP_024301814.1:n.403+93_403+95del
XM_024446047.1:c.403+93_403+95del	XP_024301815.1:n.403+93_403+95del
NM_005903.7:c.403+93_403+95del MANE Select	NP_005894.3:n.403+93_403+95del
NM_001001419.3:c.403+93_403+95del	NP_001001419.1:n.403+93_403+95del
NM_001001420.3:c.403+93_403+95del	NP_001001420.1:n.403+93_403+95del