Canonical Allele Identifier: CA355763622
Gene: CCDC50 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.191092883G>T (hg19) chr3:g.191375094G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375094G>T , CM000665.2:g.191375094G>T GRCh38
NC_000003.11:g.191092883G>T , CM000665.1:g.191092883G>T GRCh37
NC_000003.10:g.192575577G>T NCBI36
NG_008994.1:g.51010G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.481G>T MANE Select ENSP00000376249.4:p.Gly161Cys
ENST00000392456.4:c.448+5058G>T ENSP00000376250.4:n.448+5058G>T
ENST00000392455.7:c.448+5058G>T ENSP00000376249.3:n.448+5058G>T
ENST00000392456.3:c.481G>T ENSP00000376250.3:p.Gly161Cys
NM_174908.3:c.448+5058G>T NP_777568.1:n.448+5058G>T
NM_178335.2:c.481G>T NP_848018.1:p.Gly161Cys
XM_011512460.1:c.481G>T XP_011510762.1:p.Gly161Cys
NM_178335.3:c.481G>T MANE Select NP_848018.1:p.Gly161Cys
NM_174908.4:c.448+5058G>T NP_777568.1:n.448+5058G>T
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