Canonical Allele Identifier: CA743890947
Gene: GDF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1281726
ClinVar RCV Id: RCV001693710
dbSNP Id: rs3055779

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35438386_35438391dup , CM000682.2:g.35438386_35438391dup GRCh38
NC_000020.10:g.34026178_34026183dup , CM000682.1:g.34026178_34026183dup GRCh37
NC_000020.9:g.33489592_33489597dup NCBI36
NG_008076.2:g.4856_4861dup
NG_008076.3:g.21383_21388dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000374372.1:c.-241-195_-241-190dup ENSP00000363492.1:n.-241-195_-241-190dup
XM_011529075.1:c.-241-195_-241-190dup XP_011527377.1:n.-241-195_-241-190dup
XM_011529076.1:c.-241-195_-241-190dup XP_011527378.1:n.-241-195_-241-190dup
NM_001319138.1:c.-241-195_-241-190dup NP_001306067.1:n.-241-195_-241-190dup
NM_001319138.2:c.-241-195_-241-190dup NP_001306067.1:n.-241-195_-241-190dup