Canonical Allele Identifier: CA10499773

Gene: DOCK11

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.118680674C>T , CM000685.2:g.118680674C>T	GRCh38
NC_000023.10:g.117814637C>T , CM000685.1:g.117814637C>T	GRCh37
NC_000023.9:g.117698665C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_144658.4:c.5653C>T MANE Select	NP_653259.3:p.Arg1885Cys
ENST00000276202.9:c.5653C>T MANE Select	ENSP00000276202.7:p.Arg1885Cys
NM_144658.3:c.5653C>T	NP_653259.3:p.Arg1885Cys
ENST00000276202.8:c.5653C>T	ENSP00000276202.7:p.Arg1885Cys
ENST00000276204.10:c.5653C>T	ENSP00000276204.6:p.Arg1885Cys
ENST00000633080.1:c.5140C>T	ENSP00000487829.1:p.Arg1714Cys
XM_005262368.2:c.5692C>T	XP_005262425.1:p.Arg1898Cys
XM_005262368.4:c.5692C>T	XP_005262425.1:p.Arg1898Cys
XM_005262369.3:c.5599C>T	XP_005262426.1:p.Arg1867Cys
XM_005262369.5:c.5599C>T	XP_005262426.1:p.Arg1867Cys
XM_011531275.1:c.5626C>T	XP_011529577.1:p.Arg1876Cys
XM_011531276.1:c.5620C>T	XP_011529578.1:p.Arg1874Cys
XM_011531276.3:c.5620C>T	XP_011529578.1:p.Arg1874Cys
XM_011531277.1:c.4990C>T	XP_011529579.1:p.Arg1664Cys
XM_011531278.1:c.3808C>T	XP_011529580.1:p.Arg1270Cys
XM_011531278.3:c.3808C>T	XP_011529580.1:p.Arg1270Cys