Canonical Allele Identifier: CA1584853195
Gene: SMAD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136181567A= , CM000667.2:g.136181567A= GRCh38
NC_000005.9:g.135517255A= , CM000667.1:g.135517255A= GRCh37
NC_000005.8:g.135545154A= NCBI36
NG_032037.1:g.53721A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000545279.6:c.*4087A= MANE Select ENSP00000441954.2:n.*4087A=
ENST00000513418.1:c.165-5594A=
ENST00000545279.5:c.*4087A= ENSP00000441954.2:n.*4087A=
ENST00000545620.5:c.*4087A= ENSP00000446474.2:n.*4087A=
NM_001001419.2:c.*4087A= NP_001001419.1:n.*4087A=
NM_001001420.2:c.*4087A= NP_001001420.1:n.*4087A=
NM_005903.6:c.*4087A= NP_005894.3:n.*4087A=
XM_017009470.2:c.*4087A= XP_016864959.1:n.*4087A=
XM_024446046.1:c.*4087A= XP_024301814.1:n.*4087A=
XM_024446047.1:c.*4087A= XP_024301815.1:n.*4087A=
NM_005903.7:c.*4087A= MANE Select NP_005894.3:n.*4087A=
NM_001001419.3:c.*4087A= NP_001001419.1:n.*4087A=
NM_001001420.3:c.*4087A= NP_001001420.1:n.*4087A=