Canonical Allele Identifier: CA500989075

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051289T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973925T>C , CM000679.2:g.49973925T>C	GRCh38
NC_000017.10:g.48051289T>C , CM000679.1:g.48051289T>C	GRCh37
NC_000017.9:g.45406288T>C	NCBI36
NG_030592.1:g.9728T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1586T>C
ENST00000240306.5:c.705T>C MANE Select	ENSP00000240306.3:p.Ala235=
ENST00000240306.4:c.705T>C	ENSP00000240306.3:p.Ala235=
ENST00000411890.3:c.489T>C	ENSP00000410622.2:p.Ala163=
ENST00000611342.1:c.*575T>C	ENSP00000480366.1:n.*575T>C
NM_001934.3:c.489T>C	NP_001925.2:p.Ala163=
NM_138281.2:c.705T>C	NP_612138.1:p.Ala235=
XM_011524459.1:c.489T>C	XP_011522761.1:p.Ala163=
XM_017024291.1:c.489T>C	XP_016879780.1:p.Ala163=
NM_138281.3:c.705T>C MANE Select	NP_612138.1:p.Ala235=
NM_001934.4:c.489T>C	NP_001925.2:p.Ala163=