Canonical Allele Identifier: CA500630878

Gene: CCDC103 FAM187A

Linked Data

• MyVariant Identifiers: chr17:g.42979927G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44902559G>T , CM000679.2:g.44902559G>T	GRCh38
NC_000017.10:g.42979927G>T , CM000679.1:g.42979927G>T	GRCh37
NC_000017.9:g.40335453G>T	NCBI36
NG_032674.1:g.2067C>A
NG_032792.1:g.7848G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000417826.3:c.471G>T (CCDC103) MANE Select	ENSP00000391692.2:p.Pro157=
ENST00000331733.4:c.-1271G>T (FAM187A)	ENSP00000329499.4:n.-1271G>T
ENST00000357776.6:c.471G>T (CCDC103)	ENSP00000350420.2:p.Pro157=
ENST00000410006.6:c.471G>T (CCDC103)	ENSP00000387252.1:p.Pro157=
ENST00000412523.3:c.471G>T (FAM187A)	ENSP00000391869.3:p.Pro157=
ENST00000417826.2:c.471G>T (CCDC103)	ENSP00000391692.2:p.Pro157=
NM_001258395.1:c.471G>T (CCDC103)	NP_001245324.1:p.Pro157=
NM_001258396.1:c.471G>T (CCDC103)	NP_001245325.1:p.Pro157=
NM_001258397.1:c.*221G>T (CCDC103)	NP_001245326.1:n.*221G>T
NM_001258398.1:c.*160G>T (CCDC103)	NP_001245327.1:n.*160G>T
NM_001258399.1:c.*160G>T (CCDC103)	NP_001245328.1:n.*160G>T
NM_213607.2:c.471G>T (CCDC103)	NP_998772.1:p.Pro157=
NM_001258395.2:c.471G>T (CCDC103)	NP_001245324.1:p.Pro157=
NM_001258396.2:c.471G>T (CCDC103)	NP_001245325.1:p.Pro157=
NM_001258398.2:c.*160G>T (CCDC103)	NP_001245327.1:n.*160G>T
NM_001258399.2:c.*160G>T (CCDC103)	NP_001245328.1:n.*160G>T
NM_213607.3:c.471G>T (CCDC103) MANE Select	NP_998772.1:p.Pro157=
NM_001258397.3:c.*221G>T (CCDC103)	NP_001245326.1:n.*221G>T
NM_001258398.3:c.*160G>T (CCDC103)	NP_001245327.1:n.*160G>T