Canonical Allele Identifier: CA301444089

Gene: CCBE1

Linked Data

• dbSNP Id: rs562246352
• gnomAD v2: 18-57314826-C-CT
• gnomAD v3: 18-59647594-C-CT
• gnomAD v4: 18-59647594-C-CT
• MyVariant Identifiers: chr18:g.57314826_57314827insT (hg19) ; chr18:g.59647594_59647595insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.59647595dup , CM000680.2:g.59647595dup	GRCh38
NC_000018.9:g.57314827dup , CM000680.1:g.57314827dup	GRCh37
NC_000018.8:g.55465807dup	NCBI36
NG_016990.1:g.54818dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000589419.2:n.215+18481dup
ENST00000650467.2:c.212+49034dup	ENSP00000496897.2:n.212+49034dup
ENST00000695903.1:c.212+49034dup	ENSP00000512255.1:n.212+49034dup
ENST00000695904.1:c.212+49034dup	ENSP00000512259.1:n.212+49034dup
ENST00000439986.9:c.212+49034dup MANE Select	ENSP00000404464.2:n.212+49034dup
ENST00000649564.1:c.212+49034dup	ENSP00000497183.1:n.212+49034dup
ENST00000650467.1:c.90+49034dup
ENST00000439986.8:c.212+49034dup	ENSP00000404464.2:n.212+49034dup
ENST00000589419.1:c.-362+18481dup	ENSP00000467710.1:n.-362+18481dup
NM_133459.3:c.212+49034dup	NP_597716.1:n.212+49034dup
XM_005266648.2:c.212+49034dup	XP_005266705.1:n.212+49034dup
NM_133459.4:c.212+49034dup MANE Select	NP_597716.1:n.212+49034dup
XM_017025556.1:c.212+49034dup	XP_016881045.1:n.212+49034dup
XM_017025557.1:c.212+49034dup	XP_016881046.1:n.212+49034dup
XM_017025558.1:c.212+49034dup	XP_016881047.1:n.212+49034dup
XM_024451091.1:c.212+49034dup	XP_024306859.1:n.212+49034dup
XR_001753142.1:n.1051+49034dup