Canonical Allele Identifier: CA1364359731

Gene: DOCK3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.51341843T>A , CM000665.2:g.51341843T>A	GRCh38
NC_000003.11:g.51379274T>A , CM000665.1:g.51379274T>A	GRCh37
NC_000003.10:g.51354314T>A	NCBI36
NG_028012.1:g.671603T>A
NG_028012.2:g.671603T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266037.10:c.3915+458T>A MANE Select	ENSP00000266037.8:n.3915+458T>A
ENST00000266037.9:c.3915+458T>A	ENSP00000266037.8:n.3915+458T>A
NM_004947.4:c.3915+458T>A	NP_004938.1:n.3915+458T>A
XM_005264914.2:c.3915+458T>A	XP_005264971.1:n.3915+458T>A
XM_005264915.2:c.3915+458T>A	XP_005264972.1:n.3915+458T>A
XM_005264916.2:c.3888+458T>A	XP_005264973.1:n.3888+458T>A
XM_005264917.2:c.3873+458T>A	XP_005264974.1:n.3873+458T>A
XM_005264918.2:c.3768+458T>A	XP_005264975.1:n.3768+458T>A
XM_006713008.2:c.3915+458T>A	XP_006713071.1:n.3915+458T>A
XM_006713009.2:c.3915+458T>A	XP_006713072.1:n.3915+458T>A
XM_006713010.2:c.3915+458T>A	XP_006713073.1:n.3915+458T>A
XM_011533441.1:c.2880+458T>A	XP_011531743.1:n.2880+458T>A
XM_011533442.1:c.1665+458T>A	XP_011531744.1:n.1665+458T>A
XM_011533443.1:c.1227+458T>A	XP_011531745.1:n.1227+458T>A
XM_011533444.1:c.1227+458T>A	XP_011531746.1:n.1227+458T>A
XM_011533445.1:c.1053+458T>A	XP_011531747.1:n.1053+458T>A
XM_005264914.3:c.3915+458T>A	XP_005264971.1:n.3915+458T>A
XM_005264915.3:c.3915+458T>A	XP_005264972.1:n.3915+458T>A
XM_005264916.4:c.3888+458T>A	XP_005264973.1:n.3888+458T>A
XM_005264917.3:c.3873+458T>A	XP_005264974.1:n.3873+458T>A
XM_005264918.4:c.3768+458T>A	XP_005264975.1:n.3768+458T>A
XM_006713008.3:c.3915+458T>A	XP_006713071.1:n.3915+458T>A
XM_006713009.3:c.3915+458T>A	XP_006713072.1:n.3915+458T>A
XM_006713010.3:c.3915+458T>A	XP_006713073.1:n.3915+458T>A
XM_011533441.3:c.2880+458T>A	XP_011531743.1:n.2880+458T>A
XM_011533443.2:c.1227+458T>A	XP_011531745.1:n.1227+458T>A
XM_011533444.2:c.1227+458T>A	XP_011531746.1:n.1227+458T>A
XM_011533445.2:c.1053+458T>A	XP_011531747.1:n.1053+458T>A
XM_017005825.2:c.3915+458T>A	XP_016861314.1:n.3915+458T>A
XM_017005826.2:c.3915+458T>A	XP_016861315.1:n.3915+458T>A
XM_017005827.2:c.3102+458T>A	XP_016861316.1:n.3102+458T>A
XM_017005828.1:c.1053+458T>A	XP_016861317.1:n.1053+458T>A
NM_004947.5:c.3915+458T>A MANE Select	NP_004938.1:n.3915+458T>A