Canonical Allele Identifier: CA2421162
Gene: DOCK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.51260248T>C , CM000665.2:g.51260248T>C GRCh38
NC_000003.11:g.51297679T>C , CM000665.1:g.51297679T>C GRCh37
NC_000003.10:g.51272719T>C NCBI36
NG_028012.1:g.590008T>C
NG_028012.2:g.590008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266037.10:c.2277T>C MANE Select ENSP00000266037.8:p.Ser759=
ENST00000266037.9:c.2277T>C ENSP00000266037.8:p.Ser759=
NM_004947.4:c.2277T>C NP_004938.1:p.Ser759=
XM_005264914.2:c.2277T>C XP_005264971.1:p.Ser759=
XM_005264915.2:c.2277T>C XP_005264972.1:p.Ser759=
XM_005264916.2:c.2277T>C XP_005264973.1:p.Ser759=
XM_005264917.2:c.2277T>C XP_005264974.1:p.Ser759=
XM_005264918.2:c.2277T>C XP_005264975.1:p.Ser759=
XM_006713008.2:c.2277T>C XP_006713071.1:p.Ser759=
XM_006713009.2:c.2277T>C XP_006713072.1:p.Ser759=
XM_006713010.2:c.2277T>C XP_006713073.1:p.Ser759=
XM_011533441.1:c.1242T>C XP_011531743.1:p.Ser414=
XM_011533442.1:c.27T>C XP_011531744.1:p.Ser9=
XM_011533446.1:c.2277T>C XP_011531748.1:p.Ser759=
XM_005264914.3:c.2277T>C XP_005264971.1:p.Ser759=
XM_005264915.3:c.2277T>C XP_005264972.1:p.Ser759=
XM_005264916.4:c.2277T>C XP_005264973.1:p.Ser759=
XM_005264917.3:c.2277T>C XP_005264974.1:p.Ser759=
XM_005264918.4:c.2277T>C XP_005264975.1:p.Ser759=
XM_006713008.3:c.2277T>C XP_006713071.1:p.Ser759=
XM_006713009.3:c.2277T>C XP_006713072.1:p.Ser759=
XM_006713010.3:c.2277T>C XP_006713073.1:p.Ser759=
XM_011533441.3:c.1242T>C XP_011531743.1:p.Ser414=
XM_017005825.2:c.2277T>C XP_016861314.1:p.Ser759=
XM_017005826.2:c.2277T>C XP_016861315.1:p.Ser759=
XM_017005827.2:c.1464T>C XP_016861316.1:p.Ser488=
NM_004947.5:c.2277T>C MANE Select NP_004938.1:p.Ser759=