Canonical Allele Identifier: CA487828570

Gene: CCDC88C

Linked Data

• MyVariant Identifiers: chr14:g.91739094A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91272750A>G , CM000676.2:g.91272750A>G	GRCh38
NC_000014.8:g.91739094A>G , CM000676.1:g.91739094A>G	GRCh37
NC_000014.7:g.90808847A>G	NCBI36
NG_033118.1:g.150095T>C
NG_033118.2:g.150095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.5962T>C MANE Select	ENSP00000374507.6:p.Leu1988=
ENST00000331194.8:c.1396T>C	ENSP00000330332.8:p.Leu466=
ENST00000389857.10:c.5962T>C	ENSP00000374507.6:p.Leu1988=
ENST00000556726.5:c.2190T>C
NM_001080414.3:c.5962T>C	NP_001073883.2:p.Leu1988=
XM_011536796.1:c.5854T>C	XP_011535098.1:p.Leu1952=
XM_011536796.2:c.5854T>C	XP_011535098.1:p.Leu1952=
XM_017021336.1:c.3043T>C	XP_016876825.1:p.Leu1015=
NM_001080414.4:c.5962T>C MANE Select	NP_001073883.2:p.Leu1988=