Canonical Allele Identifier: CA487828668

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739161T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272817T>A , CM000676.2:g.91272817T>A	GRCh38
NC_000014.8:g.91739161T>A , CM000676.1:g.91739161T>A	GRCh37
NC_000014.7:g.90808914T>A	NCBI36
NG_033118.1:g.150028A>T
NG_033118.2:g.150028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5895A>T MANE Select	ENSP00000374507.6:p.Gly1965=
ENST00000331194.8:c.1329A>T	ENSP00000330332.8:p.Gly443=
ENST00000389857.10:c.5895A>T	ENSP00000374507.6:p.Gly1965=
ENST00000556726.5:c.2123A>T
NM_001080414.3:c.5895A>T	NP_001073883.2:p.Gly1965=
XM_011536796.1:c.5787A>T	XP_011535098.1:p.Gly1929=
XM_011536796.2:c.5787A>T	XP_011535098.1:p.Gly1929=
XM_017021336.1:c.2976A>T	XP_016876825.1:p.Gly992=
NM_001080414.4:c.5895A>T MANE Select	NP_001073883.2:p.Gly1965=