Canonical Allele Identifier: CA1971460

Gene: CDCA7

Linked Data

• dbSNP Id: rs775834708
• ExAC: 2:174231211 CTG / C
• gnomAD v2: 2-174231211-CTG-C
• gnomAD v4: 2-173366483-CTG-C
• MyVariant Identifiers: chr2:g.174231212_174231213del (hg19) ; chr2:g.173366484_173366485del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366486_173366487del , CM000664.2:g.173366486_173366487del	GRCh38
NC_000002.11:g.174231214_174231215del , CM000664.1:g.174231214_174231215del	GRCh37
NC_000002.10:g.173939460_173939461del	NCBI36
NG_047202.1:g.17470_17471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-664_799-663del	ENSP00000512251.1:n.799-664_799-663del
ENST00000695911.1:c.963+54_963+55del	ENSP00000512262.1:n.963+54_963+55del
ENST00000695912.1:c.1182+54_1182+55del	ENSP00000512263.1:n.1182+54_1182+55del
ENST00000695913.1:c.*1938+54_*1938+55del	ENSP00000512264.1:n.*1938+54_*1938+55del
ENST00000695914.1:c.945+54_945+55del	ENSP00000512265.1:n.945+54_945+55del
ENST00000695918.1:n.413+54_413+55del
ENST00000306721.8:c.1185+54_1185+55del MANE Select	ENSP00000306968.3:n.1185+54_1185+55del
ENST00000306721.7:c.1185+54_1185+55del	ENSP00000306968.3:n.1185+54_1185+55del
ENST00000347703.7:c.948+54_948+55del	ENSP00000272789.4:n.948+54_948+55del
ENST00000410019.3:c.822+54_822+55del	ENSP00000386833.3:n.822+54_822+55del
ENST00000410101.7:c.1053+54_1053+55del	ENSP00000386656.3:n.1053+54_1053+55del
ENST00000467411.5:n.1769-664_1769-663del
ENST00000496441.5:n.1939+54_1939+55del
NM_031942.4:c.1185+54_1185+55del	NP_114148.3:n.1185+54_1185+55del
NM_145810.2:c.948+54_948+55del	NP_665809.1:n.948+54_948+55del
XM_011511957.1:c.1104+54_1104+55del	XP_011510259.1:n.1104+54_1104+55del
XR_923034.1:n.2083+54_2083+55del
NM_031942.5:c.1185+54_1185+55del MANE Select	NP_114148.3:n.1185+54_1185+55del
NM_145810.3:c.948+54_948+55del	NP_665809.1:n.948+54_948+55del