Canonical Allele Identifier: CA537974551

Gene: CDCA7

Linked Data

• dbSNP Id: rs1314971927
• gnomAD v2: 2-174231175-G-C
• gnomAD v4: 2-173366447-G-C
• MyVariant Identifiers: chr2:g.174231175G>C (hg19) ; chr2:g.173366447G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366447G>C , CM000664.2:g.173366447G>C	GRCh38
NC_000002.11:g.174231175G>C , CM000664.1:g.174231175G>C	GRCh37
NC_000002.10:g.173939421G>C	NCBI36
NG_047202.1:g.17431G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.799-703G>C	ENSP00000512251.1:n.799-703G>C
ENST00000695911.1:c.963+15G>C	ENSP00000512262.1:n.963+15G>C
ENST00000695912.1:c.1182+15G>C	ENSP00000512263.1:n.1182+15G>C
ENST00000695913.1:c.*1938+15G>C	ENSP00000512264.1:n.*1938+15G>C
ENST00000695914.1:c.945+15G>C	ENSP00000512265.1:n.945+15G>C
ENST00000695918.1:n.413+15G>C
ENST00000306721.8:c.1185+15G>C MANE Select	ENSP00000306968.3:n.1185+15G>C
ENST00000306721.7:c.1185+15G>C	ENSP00000306968.3:n.1185+15G>C
ENST00000347703.7:c.948+15G>C	ENSP00000272789.4:n.948+15G>C
ENST00000410019.3:c.822+15G>C	ENSP00000386833.3:n.822+15G>C
ENST00000410101.7:c.1053+15G>C	ENSP00000386656.3:n.1053+15G>C
ENST00000467411.5:n.1769-703G>C
ENST00000496441.5:n.1939+15G>C
NM_031942.4:c.1185+15G>C	NP_114148.3:n.1185+15G>C
NM_145810.2:c.948+15G>C	NP_665809.1:n.948+15G>C
XM_011511957.1:c.1104+15G>C	XP_011510259.1:n.1104+15G>C
XR_923034.1:n.2083+15G>C
NM_031942.5:c.1185+15G>C MANE Select	NP_114148.3:n.1185+15G>C
NM_145810.3:c.948+15G>C	NP_665809.1:n.948+15G>C