Canonical Allele Identifier: CA2261607904

Gene: CCDC103 FAM187A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44902470G= , CM000679.2:g.44902470G=	GRCh38
NC_000017.10:g.42979838G= , CM000679.1:g.42979838G=	GRCh37
NC_000017.9:g.40335364G=	NCBI36
NG_032674.1:g.2156C=
NG_032792.1:g.7759G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417826.3:c.382G= (CCDC103) MANE Select	ENSP00000391692.2:p.Gly128=
ENST00000331733.4:c.-1360G= (FAM187A)	ENSP00000329499.4:n.-1360G=
ENST00000357776.6:c.382G= (CCDC103)	ENSP00000350420.2:p.Gly128=
ENST00000410006.6:c.382G= (CCDC103)	ENSP00000387252.1:p.Gly128=
ENST00000410027.5:c.*132G= (CCDC103)	ENSP00000386640.1:n.*132G=
ENST00000412523.3:c.382G= (FAM187A)	ENSP00000391869.3:p.Gly128=
ENST00000417826.2:c.382G= (CCDC103)	ENSP00000391692.2:p.Gly128=
NM_001258395.1:c.382G= (CCDC103)	NP_001245324.1:p.Gly128=
NM_001258396.1:c.382G= (CCDC103)	NP_001245325.1:p.Gly128=
NM_001258397.1:c.*132G= (CCDC103)	NP_001245326.1:n.*132G=
NM_001258398.1:c.*71G= (CCDC103)	NP_001245327.1:n.*71G=
NM_001258399.1:c.*71G= (CCDC103)	NP_001245328.1:n.*71G=
NM_213607.2:c.382G= (CCDC103)	NP_998772.1:p.Gly128=
NM_001258395.2:c.382G= (CCDC103)	NP_001245324.1:p.Gly128=
NM_001258396.2:c.382G= (CCDC103)	NP_001245325.1:p.Gly128=
NM_001258398.2:c.*71G= (CCDC103)	NP_001245327.1:n.*71G=
NM_001258399.2:c.*71G= (CCDC103)	NP_001245328.1:n.*71G=
NM_213607.3:c.382G= (CCDC103) MANE Select	NP_998772.1:p.Gly128=
NM_001258397.3:c.*132G= (CCDC103)	NP_001245326.1:n.*132G=
NM_001258398.3:c.*71G= (CCDC103)	NP_001245327.1:n.*71G=