Canonical Allele Identifier: CA2259487731

Gene: CDC6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40290358T= , CM000679.2:g.40290358T=	GRCh38
NC_000017.10:g.38446610T= , CM000679.1:g.38446610T=	GRCh37
NC_000017.9:g.35700136T=	NCBI36
NG_028240.1:g.7465T=
NG_028240.2:g.7480T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000209728.9:c.179-700T= MANE Select	ENSP00000209728.4:n.179-700T=
ENST00000649662.1:c.179-700T=	ENSP00000497345.1:n.179-700T=
ENST00000209728.8:c.179-700T=	ENSP00000209728.4:n.179-700T=
ENST00000473555.1:c.179-700T=	ENSP00000464047.1:n.179-700T=
ENST00000577249.1:c.179-700T=	ENSP00000463004.1:n.179-700T=
ENST00000580824.5:c.179-700T=	ENSP00000463635.1:n.179-700T=
NM_001254.3:c.179-700T=	NP_001245.1:n.179-700T=
XM_011525541.1:c.179-700T=	XP_011523843.1:n.179-700T=
XM_011525542.1:c.179-700T=	XP_011523844.1:n.179-700T=
NM_001254.4:c.179-700T= MANE Select	NP_001245.1:n.179-700T=
XM_011525541.2:c.179-700T=	XP_011523843.1:n.179-700T=