Canonical Allele Identifier: CA314131443

Gene: GDF5 GDF5-AS1

Linked Data

• dbSNP Id: rs950316163
• MyVariant Identifiers: chr20:g.34021884G>C (hg19) ; chr20:g.35434086G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35434086G>C , CM000682.2:g.35434086G>C	GRCh38
NC_000020.10:g.34021884G>C , CM000682.1:g.34021884G>C	GRCh37
NC_000020.9:g.33485298G>C	NCBI36
NG_008076.2:g.9134C>G
NG_008076.3:g.25661C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374369.8:c.1329C>G (GDF5) MANE Select	ENSP00000363489.3:p.Pro443=
ENST00000374369.7:c.1329C>G (GDF5)	ENSP00000363489.3:p.Pro443=
ENST00000374372.1:c.1329C>G (GDF5)	ENSP00000363492.1:p.Pro443=
ENST00000374375.1:c.-73G>C (GDF5-AS1)	ENSP00000363495.1:n.-73G>C
NM_000557.4:c.1329C>G (GDF5)	NP_000548.2:p.Pro443=
XM_011529075.1:c.1329C>G (GDF5)	XP_011527377.1:p.Pro443=
XM_011529076.1:c.1329C>G (GDF5)	XP_011527378.1:p.Pro443=
NM_001319138.1:c.1329C>G (GDF5)	NP_001306067.1:p.Pro443=
NM_001355428.1:c.-73G>C (GDF5-AS1)	NP_001342357.1:n.-73G>C
NM_000557.5:c.1329C>G (GDF5) MANE Select	NP_000548.2:p.Pro443=
NM_001319138.2:c.1329C>G (GDF5)	NP_001306067.1:p.Pro443=
NR_161326.1:n.370G>C (GDF5-AS1)