Canonical Allele Identifier: CA1734731871
Gene: DOCK4 HGNC NCBI
DOCK4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.111811603T>G , CM000669.2:g.111811603T>G GRCh38
NC_000007.13:g.111451659T>G , CM000669.1:g.111451659T>G GRCh37
NC_000007.12:g.111238895T>G NCBI36
NG_028060.1:g.399804A>C
NG_028060.2:g.399809A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000428084.6:c.3006+271A>C (DOCK4) MANE Select ENSP00000410746.1:n.3006+271A>C
ENST00000437633.6:c.3006+271A>C (DOCK4) ENSP00000404179.1:n.3006+271A>C
ENST00000494651.7:c.2970+271A>C (DOCK4) ENSP00000440944.3:n.2970+271A>C
ENST00000423057.6:c.1361+271A>C (DOCK4)
ENST00000428084.5:c.3006+271A>C (DOCK4) ENSP00000410746.1:n.3006+271A>C
ENST00000437633.5:c.3006+271A>C (DOCK4) ENSP00000404179.1:n.3006+271A>C
ENST00000445943.5:c.3077+271A>C (DOCK4)
ENST00000469898.1:n.139+271A>C (DOCK4)
ENST00000494651.6:c.2970+271A>C (DOCK4) ENSP00000440944.2:n.2970+271A>C
NM_014705.3:c.3006+271A>C (DOCK4) NP_055520.3:n.3006+271A>C
NR_103806.1:n.109+2990T>G (DOCK4-AS1)
XM_006716188.1:c.3006+271A>C (DOCK4) XP_006716251.1:n.3006+271A>C
XM_006716189.1:c.3006+271A>C (DOCK4) XP_006716252.1:n.3006+271A>C
XM_011516716.1:c.3006+271A>C (DOCK4) XP_011515018.1:n.3006+271A>C
XM_011516717.1:c.3006+271A>C (DOCK4) XP_011515019.1:n.3006+271A>C
NM_001363540.1:c.3006+271A>C (DOCK4) NP_001350469.1:n.3006+271A>C
XM_006716189.2:c.3006+271A>C (DOCK4) XP_006716252.1:n.3006+271A>C
XM_017012819.1:c.3099+271A>C (DOCK4) XP_016868308.1:n.3099+271A>C
XM_017012820.1:c.3099+271A>C (DOCK4) XP_016868309.1:n.3099+271A>C
XM_017012821.1:c.3099+271A>C (DOCK4) XP_016868310.1:n.3099+271A>C
XM_017012822.1:c.3039+271A>C (DOCK4) XP_016868311.1:n.3039+271A>C
XM_017012823.1:c.3099+271A>C (DOCK4) XP_016868312.1:n.3099+271A>C
XM_017012824.1:c.3099+271A>C (DOCK4) XP_016868313.1:n.3099+271A>C
XM_017012825.1:c.3099+271A>C (DOCK4) XP_016868314.1:n.3099+271A>C
XM_024447006.1:c.2778+271A>C (DOCK4) XP_024302774.1:n.2778+271A>C
NM_014705.4:c.3006+271A>C (DOCK4) NP_055520.3:n.3006+271A>C
NM_001363540.2:c.3006+271A>C (DOCK4) MANE Select NP_001350469.1:n.3006+271A>C