Canonical Allele Identifier: CA2692951892
Gene: SHOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.641174_641177del , CM000685.2:g.641174_641177del GRCh38
NC_000023.10:g.601909_601912del , CM000685.1:g.601909_601912del GRCh37
NC_000023.9:g.521909_521912del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.633+87_633+90del MANE Select ENSP00000508521.1:n.633+87_633+90del
ENST00000334060.8:c.633+87_633+90del ENSP00000335505.3:n.633+87_633+90del
ENST00000381575.6:c.633+87_633+90del ENSP00000370987.1:n.633+87_633+90del
ENST00000381578.6:c.633+87_633+90del ENSP00000370990.1:n.633+87_633+90del
ENST00000554971.6:c.633+87_633+90del ENSP00000452016.1:n.633+87_633+90del