Canonical Allele Identifier: CA412231602

Gene: SHOX

Linked Data

• MyVariant Identifiers: chrX:g.601554A>G (hg19) ; chrX:g.640819A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.640819A>G , CM000685.2:g.640819A>G	GRCh38
NC_000023.10:g.601554A>G , CM000685.1:g.601554A>G	GRCh37
NC_000023.9:g.521554A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686671.1:c.487-2A>G MANE Select	ENSP00000508521.1:n.487-2A>G
ENST00000334060.8:c.487-2A>G	ENSP00000335505.3:n.487-2A>G
ENST00000381575.6:c.487-2A>G	ENSP00000370987.1:n.487-2A>G
ENST00000381578.6:c.487-2A>G	ENSP00000370990.1:n.487-2A>G
ENST00000554971.6:c.487-2A>G	ENSP00000452016.1:n.487-2A>G