Canonical Allele Identifier: CA355763604
Gene: CCDC50 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.191092879A>T (hg19) chr3:g.191375090A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375090A>T , CM000665.2:g.191375090A>T GRCh38
NC_000003.11:g.191092879A>T , CM000665.1:g.191092879A>T GRCh37
NC_000003.10:g.192575573A>T NCBI36
NG_008994.1:g.51006A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.477A>T MANE Select ENSP00000376249.4:p.Glu159Asp
ENST00000392456.4:c.448+5054A>T ENSP00000376250.4:n.448+5054A>T
ENST00000392455.7:c.448+5054A>T ENSP00000376249.3:n.448+5054A>T
ENST00000392456.3:c.477A>T ENSP00000376250.3:p.Glu159Asp
NM_174908.3:c.448+5054A>T NP_777568.1:n.448+5054A>T
NM_178335.2:c.477A>T NP_848018.1:p.Glu159Asp
XM_011512460.1:c.477A>T XP_011510762.1:p.Glu159Asp
NM_178335.3:c.477A>T MANE Select NP_848018.1:p.Glu159Asp
NM_174908.4:c.448+5054A>T NP_777568.1:n.448+5054A>T
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Search 100 bp 3'