Canonical Allele Identifier: CA8640890

Gene: DLX4

Linked Data

• dbSNP Id: rs761130785
• ExAC: 17:48051238 T / A
• gnomAD v2: 17-48051238-T-A
• gnomAD v3: 17-49973874-T-A
• gnomAD v4: 17-49973874-T-A
• MyVariant Identifiers: chr17:g.48051238T>A (hg19) ; chr17:g.49973874T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973874T>A , CM000679.2:g.49973874T>A	GRCh38
NC_000017.10:g.48051238T>A , CM000679.1:g.48051238T>A	GRCh37
NC_000017.9:g.45406237T>A	NCBI36
NG_030592.1:g.9677T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1535T>A
ENST00000240306.5:c.654T>A MANE Select	ENSP00000240306.3:p.Tyr218Ter
ENST00000240306.4:c.654T>A	ENSP00000240306.3:p.Tyr218Ter
ENST00000411890.3:c.438T>A	ENSP00000410622.2:p.Tyr146Ter
ENST00000611342.1:c.*524T>A	ENSP00000480366.1:n.*524T>A
NM_001934.3:c.438T>A	NP_001925.2:p.Tyr146Ter
NM_138281.2:c.654T>A	NP_612138.1:p.Tyr218Ter
XM_011524459.1:c.438T>A	XP_011522761.1:p.Tyr146Ter
XM_017024291.1:c.438T>A	XP_016879780.1:p.Tyr146Ter
NM_138281.3:c.654T>A MANE Select	NP_612138.1:p.Tyr218Ter
NM_001934.4:c.438T>A	NP_001925.2:p.Tyr146Ter