Canonical Allele Identifier: CA399829356

Gene: CCDC103 FAM187A

Linked Data

• MyVariant Identifiers: chr17:g.42979928G>C (hg19) ; chr17:g.44902560G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44902560G>C , CM000679.2:g.44902560G>C	GRCh38
NC_000017.10:g.42979928G>C , CM000679.1:g.42979928G>C	GRCh37
NC_000017.9:g.40335454G>C	NCBI36
NG_032674.1:g.2066C>G
NG_032792.1:g.7849G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000417826.3:c.472G>C (CCDC103) MANE Select	ENSP00000391692.2:p.Ala158Pro
ENST00000331733.4:c.-1270G>C (FAM187A)	ENSP00000329499.4:n.-1270G>C
ENST00000357776.6:c.472G>C (CCDC103)	ENSP00000350420.2:p.Ala158Pro
ENST00000410006.6:c.472G>C (CCDC103)	ENSP00000387252.1:p.Ala158Pro
ENST00000412523.3:c.472G>C (FAM187A)	ENSP00000391869.3:p.Ala158Pro
ENST00000417826.2:c.472G>C (CCDC103)	ENSP00000391692.2:p.Ala158Pro
NM_001258395.1:c.472G>C (CCDC103)	NP_001245324.1:p.Ala158Pro
NM_001258396.1:c.472G>C (CCDC103)	NP_001245325.1:p.Ala158Pro
NM_001258397.1:c.*222G>C (CCDC103)	NP_001245326.1:n.*222G>C
NM_001258398.1:c.*161G>C (CCDC103)	NP_001245327.1:n.*161G>C
NM_001258399.1:c.*161G>C (CCDC103)	NP_001245328.1:n.*161G>C
NM_213607.2:c.472G>C (CCDC103)	NP_998772.1:p.Ala158Pro
NM_001258395.2:c.472G>C (CCDC103)	NP_001245324.1:p.Ala158Pro
NM_001258396.2:c.472G>C (CCDC103)	NP_001245325.1:p.Ala158Pro
NM_001258398.2:c.*161G>C (CCDC103)	NP_001245327.1:n.*161G>C
NM_001258399.2:c.*161G>C (CCDC103)	NP_001245328.1:n.*161G>C
NM_213607.3:c.472G>C (CCDC103) MANE Select	NP_998772.1:p.Ala158Pro
NM_001258397.3:c.*222G>C (CCDC103)	NP_001245326.1:n.*222G>C
NM_001258398.3:c.*161G>C (CCDC103)	NP_001245327.1:n.*161G>C