Canonical Allele Identifier: CA163012278
Community Standard Title: NM_005221.6(DLX5):c.356-168T>G
Gene: DLX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97022537A>C , CM000669.2:g.97022537A>C GRCh38
NC_000007.13:g.96651849A>C , CM000669.1:g.96651849A>C GRCh37
NC_000007.12:g.96489785A>C NCBI36
NG_009220.1:g.7295T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005221.6:c.356-168T>G MANE Select NP_005212.1:n.356-168T>G
ENST00000648378.1:c.356-168T>G MANE Select ENSP00000498116.1:n.356-168T>G
NM_005221.5:c.356-168T>G NP_005212.1:n.356-168T>G
ENST00000222598.4:c.356-168T>G ENSP00000222598.4:n.356-168T>G
ENST00000486603.2:c.356-168T>G ENSP00000475008.1:n.356-168T>G
ENST00000493764.1:n.560-250T>G
XM_005250185.2:c.-34T>G XP_005250242.1:n.-34T>G
XM_005250185.3:c.-34T>G XP_005250242.1:n.-34T>G
XM_011515860.1:c.356-250T>G XP_011514162.1:n.356-250T>G
XR_927389.1:n.564-168T>G