Canonical Allele Identifier: CA400168738

Gene: DLX4

Linked Data

• dbSNP Id: rs1905621127
• MyVariant Identifiers: chr17:g.48051255C>G (hg19) ; chr17:g.49973891C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973891C>G , CM000679.2:g.49973891C>G	GRCh38
NC_000017.10:g.48051255C>G , CM000679.1:g.48051255C>G	GRCh37
NC_000017.9:g.45406254C>G	NCBI36
NG_030592.1:g.9694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1552C>G
ENST00000240306.5:c.671C>G MANE Select	ENSP00000240306.3:p.Ala224Gly
ENST00000240306.4:c.671C>G	ENSP00000240306.3:p.Ala224Gly
ENST00000411890.3:c.455C>G	ENSP00000410622.2:p.Ala152Gly
ENST00000611342.1:c.*541C>G	ENSP00000480366.1:n.*541C>G
NM_001934.3:c.455C>G	NP_001925.2:p.Ala152Gly
NM_138281.2:c.671C>G	NP_612138.1:p.Ala224Gly
XM_011524459.1:c.455C>G	XP_011522761.1:p.Ala152Gly
XM_017024291.1:c.455C>G	XP_016879780.1:p.Ala152Gly
NM_138281.3:c.671C>G MANE Select	NP_612138.1:p.Ala224Gly
NM_001934.4:c.455C>G	NP_001925.2:p.Ala152Gly