Canonical Allele Identifier: CA437637532

Gene: CCDC50

Linked Data

• MyVariant Identifiers: chr3:g.191093032C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375243C>A , CM000665.2:g.191375243C>A	GRCh38
NC_000003.11:g.191093032C>A , CM000665.1:g.191093032C>A	GRCh37
NC_000003.10:g.192575726C>A	NCBI36
NG_008994.1:g.51159C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.630C>A MANE Select	ENSP00000376249.4:p.Gly210=
ENST00000392456.4:c.449-4916C>A	ENSP00000376250.4:n.449-4916C>A
ENST00000392455.7:c.449-4916C>A	ENSP00000376249.3:n.449-4916C>A
ENST00000392456.3:c.630C>A	ENSP00000376250.3:p.Gly210=
NM_174908.3:c.449-4916C>A	NP_777568.1:n.449-4916C>A
NM_178335.2:c.630C>A	NP_848018.1:p.Gly210=
XM_011512460.1:c.630C>A	XP_011510762.1:p.Gly210=
NM_178335.3:c.630C>A MANE Select	NP_848018.1:p.Gly210=
NM_174908.4:c.449-4916C>A	NP_777568.1:n.449-4916C>A