Canonical Allele Identifier: CA500989110

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051208C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973844C>T , CM000679.2:g.49973844C>T	GRCh38
NC_000017.10:g.48051208C>T , CM000679.1:g.48051208C>T	GRCh37
NC_000017.9:g.45406207C>T	NCBI36
NG_030592.1:g.9647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1505C>T
ENST00000240306.5:c.624C>T MANE Select	ENSP00000240306.3:p.Pro208=
ENST00000240306.4:c.624C>T	ENSP00000240306.3:p.Pro208=
ENST00000411890.3:c.408C>T	ENSP00000410622.2:p.Pro136=
ENST00000611342.1:c.*494C>T	ENSP00000480366.1:n.*494C>T
NM_001934.3:c.408C>T	NP_001925.2:p.Pro136=
NM_138281.2:c.624C>T	NP_612138.1:p.Pro208=
XM_011524459.1:c.408C>T	XP_011522761.1:p.Pro136=
XM_017024291.1:c.408C>T	XP_016879780.1:p.Pro136=
NM_138281.3:c.624C>T MANE Select	NP_612138.1:p.Pro208=
NM_001934.4:c.408C>T	NP_001925.2:p.Pro136=