Canonical Allele Identifier: CA1308216483

Gene: CDCA7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366483_173366485delinsCTG , CM000664.2:g.173366483_173366485delinsCTG	GRCh38
NC_000002.11:g.174231211_174231213delinsCTG , CM000664.1:g.174231211_174231213delinsCTG	GRCh37
NC_000002.10:g.173939457_173939459delinsCTG	NCBI36
NG_047202.1:g.17467_17469delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-667_799-665delinsCTG	ENSP00000512251.1:n.799-667_799-665delinsCTG
ENST00000695911.1:c.963+51_963+53delinsCTG	ENSP00000512262.1:n.963+51_963+53delinsCTG
ENST00000695912.1:c.1182+51_1182+53delinsCTG	ENSP00000512263.1:n.1182+51_1182+53delinsCTG
ENST00000695913.1:c.*1938+51_*1938+53delinsCTG	ENSP00000512264.1:n.*1938+51_*1938+53delinsCTG
ENST00000695914.1:c.945+51_945+53delinsCTG	ENSP00000512265.1:n.945+51_945+53delinsCTG
ENST00000695918.1:n.413+51_413+53delinsCTG
ENST00000306721.8:c.1185+51_1185+53delinsCTG MANE Select	ENSP00000306968.3:n.1185+51_1185+53delinsCTG
ENST00000306721.7:c.1185+51_1185+53delinsCTG	ENSP00000306968.3:n.1185+51_1185+53delinsCTG
ENST00000347703.7:c.948+51_948+53delinsCTG	ENSP00000272789.4:n.948+51_948+53delinsCTG
ENST00000410019.3:c.822+51_822+53delinsCTG	ENSP00000386833.3:n.822+51_822+53delinsCTG
ENST00000410101.7:c.1053+51_1053+53delinsCTG	ENSP00000386656.3:n.1053+51_1053+53delinsCTG
ENST00000467411.5:n.1769-667_1769-665delinsCTG
ENST00000496441.5:n.1939+51_1939+53delinsCTG
NM_031942.4:c.1185+51_1185+53delinsCTG	NP_114148.3:n.1185+51_1185+53delinsCTG
NM_145810.2:c.948+51_948+53delinsCTG	NP_665809.1:n.948+51_948+53delinsCTG
XM_011511957.1:c.1104+51_1104+53delinsCTG	XP_011510259.1:n.1104+51_1104+53delinsCTG
XR_923034.1:n.2083+51_2083+53delinsCTG
NM_031942.5:c.1185+51_1185+53delinsCTG MANE Select	NP_114148.3:n.1185+51_1185+53delinsCTG
NM_145810.3:c.948+51_948+53delinsCTG	NP_665809.1:n.948+51_948+53delinsCTG