Canonical Allele Identifier: CA2263814048
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1598148898

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974255T>G , CM000679.2:g.49974255T>G GRCh38
NC_000017.10:g.48051619T>G , CM000679.1:g.48051619T>G GRCh37
NC_000017.9:g.45406618T>G NCBI36
NG_030592.1:g.10058T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1916T>G
ENST00000240306.5:c.*312T>G MANE Select ENSP00000240306.3:n.*312T>G
ENST00000240306.4:c.*312T>G ENSP00000240306.3:n.*312T>G
ENST00000411890.3:c.*312T>G ENSP00000410622.2:n.*312T>G
ENST00000611342.1:c.*905T>G ENSP00000480366.1:n.*905T>G
NM_001934.3:c.*312T>G NP_001925.2:n.*312T>G
NM_138281.2:c.*312T>G NP_612138.1:n.*312T>G
XM_011524459.1:c.*312T>G XP_011522761.1:n.*312T>G
XM_017024291.1:c.*312T>G XP_016879780.1:n.*312T>G
NM_138281.3:c.*312T>G MANE Select NP_612138.1:n.*312T>G
NM_001934.4:c.*312T>G NP_001925.2:n.*312T>G