Canonical Allele Identifier: CA373332031

Gene: CCDC107

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658677G>A , CM000671.2:g.35658677G>A	GRCh38
NC_000009.11:g.35658674G>A , CM000671.1:g.35658674G>A	GRCh37
NC_000009.10:g.35648674G>A	NCBI36
NG_017041.1:g.4342C>T , LRG_163:g.4342C>T
NG_033120.1:g.5388G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_174923.3:c.208G>A MANE Select	NP_777583.2:p.Ala70Thr
ENST00000426546.7:c.208G>A MANE Select	ENSP00000414964.2:p.Ala70Thr
NM_001195200.1:c.208G>A	NP_001182129.1:p.Ala70Thr
NM_001195200.2:c.208G>A	NP_001182129.1:p.Ala70Thr
NM_001195201.1:c.208G>A	NP_001182130.1:p.Ala70Thr
NM_001195201.2:c.208G>A	NP_001182130.1:p.Ala70Thr
NM_001195217.1:c.208G>A	NP_001182146.1:p.Ala70Thr
NM_001195217.2:c.208G>A	NP_001182146.1:p.Ala70Thr
NM_174923.2:c.208G>A	NP_777583.2:p.Ala70Thr
ENST00000327351.6:c.208G>A	ENSP00000330327.2:p.Ala70Thr
ENST00000378406.5:c.208G>A	ENSP00000367661.1:p.Ala70Thr
ENST00000378407.7:c.208G>A	ENSP00000367662.3:p.Ala70Thr
ENST00000378409.7:c.208G>A	ENSP00000367665.3:p.Ala70Thr
ENST00000421582.2:c.208G>A	ENSP00000413003.2:p.Ala70Thr
ENST00000426546.6:c.208G>A	ENSP00000414964.2:p.Ala70Thr
XM_005251403.3:c.208G>A	XP_005251460.1:p.Ala70Thr
XM_005251403.5:c.208G>A	XP_005251460.1:p.Ala70Thr
XR_929218.1:n.306G>A
XR_929218.3:n.284G>A