Canonical Allele Identifier: CA14828645
Community Standard Title: NM_000557.5(GDF5):c.631+359T=
Gene: GDF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35436939A= , CM000682.2:g.35436939A= GRCh38
NG_008076.2:g.6281T=
NG_008076.3:g.22808T=

Transcript Alleles

HGVS Amino-acid Change
NM_000557.5:c.631+359T= MANE Select NP_000548.2:n.631+359T=
ENST00000374369.8:c.631+359T= MANE Select ENSP00000363489.3:n.631+359T=
NM_000557.4:c.631+359T= NP_000548.2:n.631+359T=
NM_001319138.1:c.631+359T= NP_001306067.1:n.631+359T=
NM_001319138.2:c.631+359T= NP_001306067.1:n.631+359T=
ENST00000374369.7:c.631+359T= ENSP00000363489.3:n.631+359T=
ENST00000374372.1:c.631+359T= ENSP00000363492.1:n.631+359T=
XM_011529075.1:c.631+359T= XP_011527377.1:n.631+359T=
XM_011529076.1:c.631+359T= XP_011527378.1:n.631+359T=