Canonical Allele Identifier: CA951808897

Gene: CCDC63

Linked Data

• dbSNP Id: rs2071502189
• gnomAD v3: 12-110902591-T-G
• gnomAD v4: 12-110902591-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110902591T>G , CM000674.2:g.110902591T>G	GRCh38
NC_000012.11:g.111340395T>G , CM000674.1:g.111340395T>G	GRCh37
NC_000012.10:g.109824778T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308208.10:c.1343-1997T>G MANE Select	ENSP00000312399.5:n.1343-1997T>G
ENST00000308208.9:c.1343-1997T>G	ENSP00000312399.5:n.1343-1997T>G
ENST00000545036.5:c.1223-1997T>G	ENSP00000445881.1:n.1223-1997T>G
ENST00000552694.1:c.1106-1997T>G	ENSP00000450217.1:n.1106-1997T>G
NM_001286243.1:c.1223-1997T>G	NP_001273172.1:n.1223-1997T>G
NM_001286244.1:c.1106-1997T>G	NP_001273173.1:n.1106-1997T>G
NM_152591.2:c.1343-1997T>G	NP_689804.1:n.1343-1997T>G
XM_006719262.1:c.1343-1997T>G	XP_006719325.1:n.1343-1997T>G
XM_006719263.2:c.1343-1997T>G	XP_006719326.1:n.1343-1997T>G
XM_011537999.1:c.1343-1997T>G	XP_011536301.1:n.1343-1997T>G
XM_011538000.1:c.1343-1997T>G	XP_011536302.1:n.1343-1997T>G
XM_011538001.1:c.1343-1997T>G	XP_011536303.1:n.1343-1997T>G
XM_011538001.2:c.1343-1997T>G	XP_011536303.1:n.1343-1997T>G
NM_001286243.2:c.1223-1997T>G	NP_001273172.1:n.1223-1997T>G
NM_001286244.2:c.1106-1997T>G	NP_001273173.1:n.1106-1997T>G
NM_152591.3:c.1343-1997T>G MANE Select	NP_689804.1:n.1343-1997T>G