Canonical Allele Identifier: CA414162303

Gene: DOCK11

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.118671066G>C , CM000685.2:g.118671066G>C	GRCh38
NC_000023.10:g.117805029G>C , CM000685.1:g.117805029G>C	GRCh37
NC_000023.9:g.117689057G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_144658.4:c.5120G>C MANE Select	NP_653259.3:p.Trp1707Ser
ENST00000276202.9:c.5120G>C MANE Select	ENSP00000276202.7:p.Trp1707Ser
NM_144658.3:c.5120G>C	NP_653259.3:p.Trp1707Ser
ENST00000276202.8:c.5120G>C	ENSP00000276202.7:p.Trp1707Ser
ENST00000276204.10:c.5120G>C	ENSP00000276204.6:p.Trp1707Ser
ENST00000633080.1:c.4607G>C	ENSP00000487829.1:p.Trp1536Ser
XM_005262368.2:c.5159G>C	XP_005262425.1:p.Trp1720Ser
XM_005262368.4:c.5159G>C	XP_005262425.1:p.Trp1720Ser
XM_005262369.3:c.5066G>C	XP_005262426.1:p.Trp1689Ser
XM_005262369.5:c.5066G>C	XP_005262426.1:p.Trp1689Ser
XM_011531275.1:c.5093G>C	XP_011529577.1:p.Trp1698Ser
XM_011531276.1:c.5087G>C	XP_011529578.1:p.Trp1696Ser
XM_011531276.3:c.5087G>C	XP_011529578.1:p.Trp1696Ser
XM_011531277.1:c.4457G>C	XP_011529579.1:p.Trp1486Ser
XM_011531278.1:c.3275G>C	XP_011529580.1:p.Trp1092Ser
XM_011531278.3:c.3275G>C	XP_011529580.1:p.Trp1092Ser