Canonical Allele Identifier: CA500988985

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051220C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973856C>G , CM000679.2:g.49973856C>G	GRCh38
NC_000017.10:g.48051220C>G , CM000679.1:g.48051220C>G	GRCh37
NC_000017.9:g.45406219C>G	NCBI36
NG_030592.1:g.9659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1517C>G
ENST00000240306.5:c.636C>G MANE Select	ENSP00000240306.3:p.Thr212=
ENST00000240306.4:c.636C>G	ENSP00000240306.3:p.Thr212=
ENST00000411890.3:c.420C>G	ENSP00000410622.2:p.Thr140=
ENST00000611342.1:c.*506C>G	ENSP00000480366.1:n.*506C>G
NM_001934.3:c.420C>G	NP_001925.2:p.Thr140=
NM_138281.2:c.636C>G	NP_612138.1:p.Thr212=
XM_011524459.1:c.420C>G	XP_011522761.1:p.Thr140=
XM_017024291.1:c.420C>G	XP_016879780.1:p.Thr140=
NM_138281.3:c.636C>G MANE Select	NP_612138.1:p.Thr212=
NM_001934.4:c.420C>G	NP_001925.2:p.Thr140=