Canonical Allele Identifier: CA2411389935
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.641224A= , CM000685.2:g.641224A= GRCh38
NC_000023.10:g.601959A= , CM000685.1:g.601959A= GRCh37
NC_000023.9:g.521959A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686671.1:c.633+137A= MANE Select ENSP00000508521.1:n.633+137A=
ENST00000334060.8:c.633+137A= ENSP00000335505.3:n.633+137A=
ENST00000381575.6:c.633+137A= ENSP00000370987.1:n.633+137A=
ENST00000381578.6:c.633+137A= ENSP00000370990.1:n.633+137A=
ENST00000554971.6:c.633+137A= ENSP00000452016.1:n.633+137A=