Canonical Allele Identifier: CA208521952

Gene: CABCOCO1

Linked Data

• dbSNP Id: rs902160661
• gnomAD v3: 10-61764928-C-T
• gnomAD v4: 10-61764928-C-T
• MyVariant Identifiers: chr10:g.63524686C>T (hg19) ; chr10:g.61764928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61764928C>T , CM000672.2:g.61764928C>T	GRCh38
NC_000010.10:g.63524686C>T , CM000672.1:g.63524686C>T	GRCh37
NC_000010.9:g.63194692C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000648843.3:c.817-1011C>T MANE Select	ENSP00000496918.2:n.817-1011C>T
ENST00000330194.2:c.553-1011C>T	ENSP00000328698.2:n.553-1011C>T
NM_173554.2:c.553-1011C>T	NP_775825.1:n.553-1011C>T
XM_005269598.2:c.679-1011C>T	XP_005269655.1:n.679-1011C>T
XM_005269599.3:c.679-1011C>T	XP_005269656.1:n.679-1011C>T
XM_005269600.3:c.553-1011C>T	XP_005269657.1:n.553-1011C>T
XM_006717690.2:c.817-1011C>T	XP_006717753.1:n.817-1011C>T
NM_001366905.1:c.553-1011C>T	NP_001353834.1:n.553-1011C>T
NM_001366906.1:c.817-1011C>T	NP_001353835.1:n.817-1011C>T
NM_001366908.1:c.679-1011C>T	NP_001353837.1:n.679-1011C>T
XM_005269598.3:c.679-1011C>T	XP_005269655.1:n.679-1011C>T
NM_001366905.2:c.553-1011C>T	NP_001353834.1:n.553-1011C>T
NM_001366906.2:c.817-1011C>T MANE Select	NP_001353835.1:n.817-1011C>T
NM_001366908.2:c.679-1011C>T	NP_001353837.1:n.679-1011C>T
NM_173554.3:c.553-1011C>T	NP_775825.1:n.553-1011C>T