Canonical Allele Identifier: CA2638666353

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974134-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974134T>C , CM000679.2:g.49974134T>C	GRCh38
NC_000017.10:g.48051498T>C , CM000679.1:g.48051498T>C	GRCh37
NC_000017.9:g.45406497T>C	NCBI36
NG_030592.1:g.9937T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1795T>C
ENST00000240306.5:c.*191T>C MANE Select	ENSP00000240306.3:n.*191T>C
ENST00000240306.4:c.*191T>C	ENSP00000240306.3:n.*191T>C
ENST00000411890.3:c.*191T>C	ENSP00000410622.2:n.*191T>C
ENST00000611342.1:c.*784T>C	ENSP00000480366.1:n.*784T>C
NM_001934.3:c.*191T>C	NP_001925.2:n.*191T>C
NM_138281.2:c.*191T>C	NP_612138.1:n.*191T>C
XM_011524459.1:c.*191T>C	XP_011522761.1:n.*191T>C
XM_017024291.1:c.*191T>C	XP_016879780.1:n.*191T>C
NM_138281.3:c.*191T>C MANE Select	NP_612138.1:n.*191T>C
NM_001934.4:c.*191T>C	NP_001925.2:n.*191T>C