Canonical Allele Identifier: CA400168801

Gene: DLX4

Linked Data

• gnomAD v4: 17-49973905-C-T
• MyVariant Identifiers: chr17:g.48051269C>T (hg19) ; chr17:g.49973905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973905C>T , CM000679.2:g.49973905C>T	GRCh38
NC_000017.10:g.48051269C>T , CM000679.1:g.48051269C>T	GRCh37
NC_000017.9:g.45406268C>T	NCBI36
NG_030592.1:g.9708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1566C>T
ENST00000240306.5:c.685C>T MANE Select	ENSP00000240306.3:p.His229Tyr
ENST00000240306.4:c.685C>T	ENSP00000240306.3:p.His229Tyr
ENST00000411890.3:c.469C>T	ENSP00000410622.2:p.His157Tyr
ENST00000611342.1:c.*555C>T	ENSP00000480366.1:n.*555C>T
NM_001934.3:c.469C>T	NP_001925.2:p.His157Tyr
NM_138281.2:c.685C>T	NP_612138.1:p.His229Tyr
XM_011524459.1:c.469C>T	XP_011522761.1:p.His157Tyr
XM_017024291.1:c.469C>T	XP_016879780.1:p.His157Tyr
NM_138281.3:c.685C>T MANE Select	NP_612138.1:p.His229Tyr
NM_001934.4:c.469C>T	NP_001925.2:p.His157Tyr