Canonical Allele Identifier: CA760834610

Gene: CDCA7

Linked Data

• dbSNP Id: rs1279520999
• MyVariant Identifiers: chr2:g.174230842_174230843del (hg19) ; chr2:g.173366114_173366115del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366114_173366115del , CM000664.2:g.173366114_173366115del	GRCh38
NC_000002.11:g.174230842_174230843del , CM000664.1:g.174230842_174230843del	GRCh37
NC_000002.10:g.173939088_173939089del	NCBI36
NG_047202.1:g.17098_17099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+522_798+523del	ENSP00000512251.1:n.798+522_798+523del
ENST00000695911.1:c.814-169_814-168del	ENSP00000512262.1:n.814-169_814-168del
ENST00000695912.1:c.1033-169_1033-168del	ENSP00000512263.1:n.1033-169_1033-168del
ENST00000695913.1:c.*1620_*1621del	ENSP00000512264.1:n.*1620_*1621del
ENST00000695914.1:c.796-169_796-168del	ENSP00000512265.1:n.796-169_796-168del
ENST00000695918.1:n.264-169_264-168del
ENST00000306721.8:c.1036-169_1036-168del MANE Select	ENSP00000306968.3:n.1036-169_1036-168del
ENST00000306721.7:c.1036-169_1036-168del	ENSP00000306968.3:n.1036-169_1036-168del
ENST00000347703.7:c.799-169_799-168del	ENSP00000272789.4:n.799-169_799-168del
ENST00000410019.3:c.673-169_673-168del	ENSP00000386833.3:n.673-169_673-168del
ENST00000410101.7:c.904-169_904-168del	ENSP00000386656.3:n.904-169_904-168del
ENST00000467411.5:n.1768+522_1768+523del
ENST00000496441.5:n.1790-169_1790-168del
NM_031942.4:c.1036-169_1036-168del	NP_114148.3:n.1036-169_1036-168del
NM_145810.2:c.799-169_799-168del	NP_665809.1:n.799-169_799-168del
XM_011511957.1:c.955-169_955-168del	XP_011510259.1:n.955-169_955-168del
XR_923034.1:n.1934-169_1934-168del
NM_031942.5:c.1036-169_1036-168del MANE Select	NP_114148.3:n.1036-169_1036-168del
NM_145810.3:c.799-169_799-168del	NP_665809.1:n.799-169_799-168del