Canonical Allele Identifier: CA1998829151

Gene: C11orf65

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108369261G= , CM000673.2:g.108369261G=	GRCh38
NC_000011.9:g.108239988G= , CM000673.1:g.108239988G=	GRCh37
NC_000011.8:g.107745198G=	NCBI36
NG_009830.1:g.151430G= , LRG_135:g.151430G=
NG_054724.1:g.105572C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524755.5:c.226+23947C=
ENST00000525729.5:c.640+16659C=	ENSP00000433395.1:n.640+16659C=
ENST00000526725.1:n.271+23947C=
ENST00000527531.5:c.*2-13152C=	ENSP00000431706.1:n.*2-13152C=
ENST00000615746.4:c.*2-13152C=	ENSP00000483537.1:n.*2-13152C=
XM_005271414.3:c.787+16659C=	XP_005271471.1:n.787+16659C=
XM_005271415.3:c.731+23947C=	XP_005271472.1:n.731+23947C=
XM_011542640.1:c.787+16659C=	XP_011540942.1:n.787+16659C=
XM_011542642.1:c.732-20188C=	XP_011540944.1:n.732-20188C=
XM_011542643.1:c.731+23947C=	XP_011540945.1:n.731+23947C=
NM_001330368.1:c.640+16659C=	NP_001317297.1:n.640+16659C=
NM_001351110.1:c.694+16659C=	NP_001338039.1:n.694+16659C=
NR_147053.2:n.1107-13152C=
XM_005271414.4:c.787+16659C=	XP_005271471.1:n.787+16659C=
XM_005271415.4:c.731+23947C=	XP_005271472.1:n.731+23947C=
XM_011542640.2:c.787+16659C=	XP_011540942.1:n.787+16659C=
XM_011542643.2:c.731+23947C=	XP_011540945.1:n.731+23947C=
XM_017017247.1:c.903+13799C=	XP_016872736.1:n.903+13799C=
NM_001330368.2:c.640+16659C=	NP_001317297.1:n.640+16659C=
NM_001351110.2:c.694+16659C=	NP_001338039.1:n.694+16659C=
NR_147053.3:n.1105-13152C=