Canonical Allele Identifier: CA2516167528

Gene: CCDC63

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110902569_110902597del , CM000674.2:g.110902569_110902597del	GRCh38
NC_000012.11:g.111340373_111340401del , CM000674.1:g.111340373_111340401del	GRCh37
NC_000012.10:g.109824756_109824784del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308208.10:c.1343-2019_1343-1991del MANE Select	ENSP00000312399.5:n.1343-2019_1343-1991del
ENST00000308208.9:c.1343-2019_1343-1991del	ENSP00000312399.5:n.1343-2019_1343-1991del
ENST00000545036.5:c.1223-2019_1223-1991del	ENSP00000445881.1:n.1223-2019_1223-1991del
ENST00000552694.1:c.1106-2019_1106-1991del	ENSP00000450217.1:n.1106-2019_1106-1991del
NM_001286243.1:c.1223-2019_1223-1991del	NP_001273172.1:n.1223-2019_1223-1991del
NM_001286244.1:c.1106-2019_1106-1991del	NP_001273173.1:n.1106-2019_1106-1991del
NM_152591.2:c.1343-2019_1343-1991del	NP_689804.1:n.1343-2019_1343-1991del
XM_006719262.1:c.1343-2019_1343-1991del	XP_006719325.1:n.1343-2019_1343-1991del
XM_006719263.2:c.1343-2019_1343-1991del	XP_006719326.1:n.1343-2019_1343-1991del
XM_011537999.1:c.1343-2019_1343-1991del	XP_011536301.1:n.1343-2019_1343-1991del
XM_011538000.1:c.1343-2019_1343-1991del	XP_011536302.1:n.1343-2019_1343-1991del
XM_011538001.1:c.1343-2019_1343-1991del	XP_011536303.1:n.1343-2019_1343-1991del
XM_011538001.2:c.1343-2019_1343-1991del	XP_011536303.1:n.1343-2019_1343-1991del
NM_001286243.2:c.1223-2019_1223-1991del	NP_001273172.1:n.1223-2019_1223-1991del
NM_001286244.2:c.1106-2019_1106-1991del	NP_001273173.1:n.1106-2019_1106-1991del
NM_152591.3:c.1343-2019_1343-1991del MANE Select	NP_689804.1:n.1343-2019_1343-1991del