Canonical Allele Identifier: CA2411385689
Gene: SHOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.634657C= , CM000685.2:g.634657C= GRCh38
NC_000023.10:g.595392C= , CM000685.1:g.595392C= GRCh37
NC_000023.9:g.515392C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686671.1:c.317C= MANE Select ENSP00000508521.1:p.Ser106=
ENST00000334060.8:c.317C= ENSP00000335505.3:p.Ser106=
ENST00000381575.6:c.317C= ENSP00000370987.1:p.Ser106=
ENST00000381578.6:c.317C= ENSP00000370990.1:p.Ser106=
ENST00000554971.6:c.317C= ENSP00000452016.1:p.Ser106=