Canonical Allele Identifier: CA355764049

Gene: CCDC50

Linked Data

• gnomAD v4: 3-191375199-C-A
• MyVariant Identifiers: chr3:g.191092988C>A (hg19) ; chr3:g.191375199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375199C>A , CM000665.2:g.191375199C>A	GRCh38
NC_000003.11:g.191092988C>A , CM000665.1:g.191092988C>A	GRCh37
NC_000003.10:g.192575682C>A	NCBI36
NG_008994.1:g.51115C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.586C>A MANE Select	ENSP00000376249.4:p.Gln196Lys
ENST00000392456.4:c.449-4960C>A	ENSP00000376250.4:n.449-4960C>A
ENST00000392455.7:c.449-4960C>A	ENSP00000376249.3:n.449-4960C>A
ENST00000392456.3:c.586C>A	ENSP00000376250.3:p.Gln196Lys
NM_174908.3:c.449-4960C>A	NP_777568.1:n.449-4960C>A
NM_178335.2:c.586C>A	NP_848018.1:p.Gln196Lys
XM_011512460.1:c.586C>A	XP_011510762.1:p.Gln196Lys
NM_178335.3:c.586C>A MANE Select	NP_848018.1:p.Gln196Lys
NM_174908.4:c.449-4960C>A	NP_777568.1:n.449-4960C>A