Canonical Allele Identifier: CA500630869

Gene: CCDC103 FAM187A

Linked Data

• MyVariant Identifiers: chr17:g.42979921G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44902553G>A , CM000679.2:g.44902553G>A	GRCh38
NC_000017.10:g.42979921G>A , CM000679.1:g.42979921G>A	GRCh37
NC_000017.9:g.40335447G>A	NCBI36
NG_032674.1:g.2073C>T
NG_032792.1:g.7842G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000417826.3:c.465G>A (CCDC103) MANE Select	ENSP00000391692.2:p.Val155=
ENST00000331733.4:c.-1277G>A (FAM187A)	ENSP00000329499.4:n.-1277G>A
ENST00000357776.6:c.465G>A (CCDC103)	ENSP00000350420.2:p.Val155=
ENST00000410006.6:c.465G>A (CCDC103)	ENSP00000387252.1:p.Val155=
ENST00000412523.3:c.465G>A (FAM187A)	ENSP00000391869.3:p.Val155=
ENST00000417826.2:c.465G>A (CCDC103)	ENSP00000391692.2:p.Val155=
NM_001258395.1:c.465G>A (CCDC103)	NP_001245324.1:p.Val155=
NM_001258396.1:c.465G>A (CCDC103)	NP_001245325.1:p.Val155=
NM_001258397.1:c.*215G>A (CCDC103)	NP_001245326.1:n.*215G>A
NM_001258398.1:c.*154G>A (CCDC103)	NP_001245327.1:n.*154G>A
NM_001258399.1:c.*154G>A (CCDC103)	NP_001245328.1:n.*154G>A
NM_213607.2:c.465G>A (CCDC103)	NP_998772.1:p.Val155=
NM_001258395.2:c.465G>A (CCDC103)	NP_001245324.1:p.Val155=
NM_001258396.2:c.465G>A (CCDC103)	NP_001245325.1:p.Val155=
NM_001258398.2:c.*154G>A (CCDC103)	NP_001245327.1:n.*154G>A
NM_001258399.2:c.*154G>A (CCDC103)	NP_001245328.1:n.*154G>A
NM_213607.3:c.465G>A (CCDC103) MANE Select	NP_998772.1:p.Val155=
NM_001258397.3:c.*215G>A (CCDC103)	NP_001245326.1:n.*215G>A
NM_001258398.3:c.*154G>A (CCDC103)	NP_001245327.1:n.*154G>A