Canonical Allele Identifier: CA626475074

Gene: DLX4

Linked Data

• dbSNP Id: rs901442853
• gnomAD v2: 17-48051695-A-C
• gnomAD v3: 17-49974331-A-C
• gnomAD v4: 17-49974331-A-C
• MyVariant Identifiers: chr17:g.48051695A>C (hg19) ; chr17:g.49974331A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974331A>C , CM000679.2:g.49974331A>C	GRCh38
NC_000017.10:g.48051695A>C , CM000679.1:g.48051695A>C	GRCh37
NC_000017.9:g.45406694A>C	NCBI36
NG_030592.1:g.10134A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1992A>C
ENST00000240306.5:c.*388A>C MANE Select	ENSP00000240306.3:n.*388A>C
ENST00000240306.4:c.*388A>C	ENSP00000240306.3:n.*388A>C
ENST00000411890.3:c.*388A>C	ENSP00000410622.2:n.*388A>C
ENST00000611342.1:c.*981A>C	ENSP00000480366.1:n.*981A>C
NM_001934.3:c.*388A>C	NP_001925.2:n.*388A>C
NM_138281.2:c.*388A>C	NP_612138.1:n.*388A>C
XM_011524459.1:c.*388A>C	XP_011522761.1:n.*388A>C
XM_017024291.1:c.*388A>C	XP_016879780.1:n.*388A>C
NM_138281.3:c.*388A>C MANE Select	NP_612138.1:n.*388A>C
NM_001934.4:c.*388A>C	NP_001925.2:n.*388A>C