Canonical Allele Identifier: CA993523686
Gene: DOCK6 HGNC NCBI

Linked Data

dbSNP Id: rs12979813

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11232027A>C , CM000681.2:g.11232027A>C GRCh38
NC_000019.9:g.11342703A>C , CM000681.1:g.11342703A>C GRCh37
NC_000019.8:g.11203703A>C NCBI36
NG_031953.1:g.35466T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000587656.6:c.2823+158T>G ENSP00000468638.2:n.2823+158T>G
ENST00000294618.12:c.2718+1176T>G MANE Select ENSP00000294618.6:n.2718+1176T>G
ENST00000294618.11:c.2718+1176T>G ENSP00000294618.6:n.2718+1176T>G
ENST00000585904.1:c.426+158T>G ENSP00000465767.1:n.426+158T>G
ENST00000587656.5:c.583+158T>G
ENST00000590680.5:c.1061+1176T>G
NM_020812.3:c.2718+1176T>G NP_065863.2:n.2718+1176T>G
XM_005260000.2:c.2823+158T>G XP_005260057.1:n.2823+158T>G
XM_005260001.2:c.2823+158T>G XP_005260058.1:n.2823+158T>G
XM_006722804.2:c.54+1012T>G XP_006722867.1:n.54+1012T>G
XM_011528150.1:c.2856+158T>G XP_011526452.1:n.2856+158T>G
XM_011528151.1:c.2751+1176T>G XP_011526453.1:n.2751+1176T>G
XM_011528152.1:c.2751+1176T>G XP_011526454.1:n.2751+1176T>G
XM_011528153.1:c.2856+158T>G XP_011526455.1:n.2856+158T>G
XR_936195.1:n.2917+158T>G
XR_936196.1:n.2812+1176T>G
XR_936197.1:n.2917+158T>G
XR_936198.1:n.2812+1176T>G
XM_006722804.3:c.54+1012T>G XP_006722867.1:n.54+1012T>G
NM_001367830.1:c.2823+158T>G NP_001354759.1:n.2823+158T>G
NM_020812.4:c.2718+1176T>G MANE Select NP_065863.2:n.2718+1176T>G