Canonical Allele Identifier: CA14422303
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1058562

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974300T>C , CM000679.2:g.49974300T>C GRCh38
NC_000017.10:g.48051664T>C , CM000679.1:g.48051664T>C GRCh37
NC_000017.9:g.45406663T>C NCBI36
NG_030592.1:g.10103T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1961T>C
ENST00000240306.5:c.*357T>C MANE Select ENSP00000240306.3:n.*357T>C
ENST00000240306.4:c.*357T>C ENSP00000240306.3:n.*357T>C
ENST00000411890.3:c.*357T>C ENSP00000410622.2:n.*357T>C
ENST00000611342.1:c.*950T>C ENSP00000480366.1:n.*950T>C
NM_001934.3:c.*357T>C NP_001925.2:n.*357T>C
NM_138281.2:c.*357T>C NP_612138.1:n.*357T>C
XM_011524459.1:c.*357T>C XP_011522761.1:n.*357T>C
XM_017024291.1:c.*357T>C XP_016879780.1:n.*357T>C
NM_138281.3:c.*357T>C MANE Select NP_612138.1:n.*357T>C
NM_001934.4:c.*357T>C NP_001925.2:n.*357T>C