Canonical Allele Identifier: CA510481711
Gene: GDF5 HGNC NCBI
GDF5-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.34022001T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35434203T>C , CM000682.2:g.35434203T>C GRCh38
NC_000020.10:g.34022001T>C , CM000682.1:g.34022001T>C GRCh37
NC_000020.9:g.33485415T>C NCBI36
NG_008076.2:g.9017A>G
NG_008076.3:g.25544A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374369.8:c.1212A>G (GDF5) MANE Select ENSP00000363489.3:p.Ala404=
ENST00000374369.7:c.1212A>G (GDF5) ENSP00000363489.3:p.Ala404=
ENST00000374372.1:c.1212A>G (GDF5) ENSP00000363492.1:p.Ala404=
ENST00000374375.1:c.45T>C (GDF5-AS1) ENSP00000363495.1:p.Ser15=
NM_000557.4:c.1212A>G (GDF5) NP_000548.2:p.Ala404=
XM_011529075.1:c.1212A>G (GDF5) XP_011527377.1:p.Ala404=
XM_011529076.1:c.1212A>G (GDF5) XP_011527378.1:p.Ala404=
NM_001319138.1:c.1212A>G (GDF5) NP_001306067.1:p.Ala404=
NM_001355428.1:c.45T>C (GDF5-AS1) NP_001342357.1:p.Ser15=
NM_000557.5:c.1212A>G (GDF5) MANE Select NP_000548.2:p.Ala404=
NM_001319138.2:c.1212A>G (GDF5) NP_001306067.1:p.Ala404=
NR_161326.1:n.487T>C (GDF5-AS1)