Canonical Allele Identifier: CA2629115033
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066456_67066465del , CM000677.2:g.67066456_67066465del GRCh38
NC_000015.9:g.67358794_67358803del , CM000677.1:g.67358794_67358803del GRCh37
NC_000015.8:g.65145848_65145857del NCBI36
NG_011990.1:g.5600_5609del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2512_-110+2521del ENSP00000453082.2:n.-110+2512_-110+2521del
ENST00000560424.2:c.206+96_206+105del ENSP00000455540.2:n.206+96_206+105del
ENST00000327367.9:c.206+96_206+105del MANE Select ENSP00000332973.4:n.206+96_206+105del
ENST00000327367.8:c.206+96_206+105del ENSP00000332973.4:n.206+96_206+105del
ENST00000559460.5:c.-110+2512_-110+2521del ENSP00000453082.1:n.-110+2512_-110+2521del
NM_005902.3:c.206+96_206+105del NP_005893.1:n.206+96_206+105del
XM_011521559.1:c.206+96_206+105del XP_011519861.1:n.206+96_206+105del
XM_011521559.3:c.206+96_206+105del XP_011519861.1:n.206+96_206+105del
NM_005902.4:c.206+96_206+105del MANE Select NP_005893.1:n.206+96_206+105del