Canonical Allele Identifier: CA500989066

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051172C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973808C>A , CM000679.2:g.49973808C>A	GRCh38
NC_000017.10:g.48051172C>A , CM000679.1:g.48051172C>A	GRCh37
NC_000017.9:g.45406171C>A	NCBI36
NG_030592.1:g.9611C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1469C>A
ENST00000240306.5:c.588C>A MANE Select	ENSP00000240306.3:p.Pro196=
ENST00000240306.4:c.588C>A	ENSP00000240306.3:p.Pro196=
ENST00000411890.3:c.372C>A	ENSP00000410622.2:p.Pro124=
ENST00000611342.1:c.*458C>A	ENSP00000480366.1:n.*458C>A
NM_001934.3:c.372C>A	NP_001925.2:p.Pro124=
NM_138281.2:c.588C>A	NP_612138.1:p.Pro196=
XM_011524459.1:c.372C>A	XP_011522761.1:p.Pro124=
XM_017024291.1:c.372C>A	XP_016879780.1:p.Pro124=
NM_138281.3:c.588C>A MANE Select	NP_612138.1:p.Pro196=
NM_001934.4:c.372C>A	NP_001925.2:p.Pro124=