Canonical Allele Identifier: CA355764159
Gene: CCDC50 HGNC NCBI

Linked Data

dbSNP Id: rs1713056725

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375251G>C , CM000665.2:g.191375251G>C GRCh38
NC_000003.11:g.191093040G>C , CM000665.1:g.191093040G>C GRCh37
NC_000003.10:g.192575734G>C NCBI36
NG_008994.1:g.51167G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.638G>C MANE Select ENSP00000376249.4:p.Arg213Thr
ENST00000392456.4:c.449-4908G>C ENSP00000376250.4:n.449-4908G>C
ENST00000392455.7:c.449-4908G>C ENSP00000376249.3:n.449-4908G>C
ENST00000392456.3:c.638G>C ENSP00000376250.3:p.Arg213Thr
NM_174908.3:c.449-4908G>C NP_777568.1:n.449-4908G>C
NM_178335.2:c.638G>C NP_848018.1:p.Arg213Thr
XM_011512460.1:c.638G>C XP_011510762.1:p.Arg213Thr
NM_178335.3:c.638G>C MANE Select NP_848018.1:p.Arg213Thr
NM_174908.4:c.449-4908G>C NP_777568.1:n.449-4908G>C