Canonical Allele Identifier: CA390623626

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91772248T>C (hg19) ; chr14:g.91305904T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305904T>C , CM000676.2:g.91305904T>C	GRCh38
NC_000014.8:g.91772248T>C , CM000676.1:g.91772248T>C	GRCh37
NC_000014.7:g.90842001T>C	NCBI36
NG_033118.1:g.116941A>G
NG_033118.2:g.116941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3218A>G MANE Select	ENSP00000374507.6:p.Lys1073Arg
ENST00000389857.10:c.3218A>G	ENSP00000374507.6:p.Lys1073Arg
NM_001080414.3:c.3218A>G	NP_001073883.2:p.Lys1073Arg
XM_005267691.3:c.3218A>G	XP_005267748.1:p.Lys1073Arg
XM_011536796.1:c.3110A>G	XP_011535098.1:p.Lys1037Arg
XR_429316.2:n.3346A>G
XR_943459.1:n.3346A>G
XM_005267691.5:c.3218A>G	XP_005267748.1:p.Lys1073Arg
XM_011536796.2:c.3110A>G	XP_011535098.1:p.Lys1037Arg
XM_017021335.2:c.3218A>G	XP_016876824.1:p.Lys1073Arg
XM_017021336.1:c.299A>G	XP_016876825.1:p.Lys100Arg
XR_429316.4:n.3344A>G
NM_001080414.4:c.3218A>G MANE Select	NP_001073883.2:p.Lys1073Arg