Canonical Allele Identifier: CA510481687

Gene: GDF5 GDF5-AS1

Linked Data

• ClinVar Variation Id: 2898375
• ClinVar RCV Id: RCV003726367
• MyVariant Identifiers: chr20:g.34021929G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35434131G>A , CM000682.2:g.35434131G>A	GRCh38
NC_000020.10:g.34021929G>A , CM000682.1:g.34021929G>A	GRCh37
NC_000020.9:g.33485343G>A	NCBI36
NG_008076.2:g.9089C>T
NG_008076.3:g.25616C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374369.8:c.1284C>T (GDF5) MANE Select	ENSP00000363489.3:p.His428=
ENST00000374369.7:c.1284C>T (GDF5)	ENSP00000363489.3:p.His428=
ENST00000374372.1:c.1284C>T (GDF5)	ENSP00000363492.1:p.His428=
ENST00000374375.1:c.-28G>A (GDF5-AS1)	ENSP00000363495.1:n.-28G>A
NM_000557.4:c.1284C>T (GDF5)	NP_000548.2:p.His428=
XM_011529075.1:c.1284C>T (GDF5)	XP_011527377.1:p.His428=
XM_011529076.1:c.1284C>T (GDF5)	XP_011527378.1:p.His428=
NM_001319138.1:c.1284C>T (GDF5)	NP_001306067.1:p.His428=
NM_001355428.1:c.-28G>A (GDF5-AS1)	NP_001342357.1:n.-28G>A
NM_000557.5:c.1284C>T (GDF5) MANE Select	NP_000548.2:p.His428=
NM_001319138.2:c.1284C>T (GDF5)	NP_001306067.1:p.His428=
NR_161326.1:n.415G>A (GDF5-AS1)