Canonical Allele Identifier: CA2263813982
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1905631432

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974095G>T , CM000679.2:g.49974095G>T GRCh38
NC_000017.10:g.48051459G>T , CM000679.1:g.48051459G>T GRCh37
NC_000017.9:g.45406458G>T NCBI36
NG_030592.1:g.9898G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1756G>T
ENST00000240306.5:c.*152G>T MANE Select ENSP00000240306.3:n.*152G>T
ENST00000240306.4:c.*152G>T ENSP00000240306.3:n.*152G>T
ENST00000411890.3:c.*152G>T ENSP00000410622.2:n.*152G>T
ENST00000611342.1:c.*745G>T ENSP00000480366.1:n.*745G>T
NM_001934.3:c.*152G>T NP_001925.2:n.*152G>T
NM_138281.2:c.*152G>T NP_612138.1:n.*152G>T
XM_011524459.1:c.*152G>T XP_011522761.1:n.*152G>T
XM_017024291.1:c.*152G>T XP_016879780.1:n.*152G>T
NM_138281.3:c.*152G>T MANE Select NP_612138.1:n.*152G>T
NM_001934.4:c.*152G>T NP_001925.2:n.*152G>T