Canonical Allele Identifier: CA400168684

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051243A>C (hg19) ; chr17:g.49973879A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973879A>C , CM000679.2:g.49973879A>C	GRCh38
NC_000017.10:g.48051243A>C , CM000679.1:g.48051243A>C	GRCh37
NC_000017.9:g.45406242A>C	NCBI36
NG_030592.1:g.9682A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1540A>C
ENST00000240306.5:c.659A>C MANE Select	ENSP00000240306.3:p.Asn220Thr
ENST00000240306.4:c.659A>C	ENSP00000240306.3:p.Asn220Thr
ENST00000411890.3:c.443A>C	ENSP00000410622.2:p.Asn148Thr
ENST00000611342.1:c.*529A>C	ENSP00000480366.1:n.*529A>C
NM_001934.3:c.443A>C	NP_001925.2:p.Asn148Thr
NM_138281.2:c.659A>C	NP_612138.1:p.Asn220Thr
XM_011524459.1:c.443A>C	XP_011522761.1:p.Asn148Thr
XM_017024291.1:c.443A>C	XP_016879780.1:p.Asn148Thr
NM_138281.3:c.659A>C MANE Select	NP_612138.1:p.Asn220Thr
NM_001934.4:c.443A>C	NP_001925.2:p.Asn148Thr