Canonical Allele Identifier: CA355760626

Gene: CCDC50

Linked Data

• dbSNP Id: rs1309756717
• gnomAD v2: 3-191074892-C-T
• gnomAD v4: 3-191357103-C-T
• MyVariant Identifiers: chr3:g.191074892C>T (hg19) ; chr3:g.191357103C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191357103C>T , CM000665.2:g.191357103C>T	GRCh38
NC_000003.11:g.191074892C>T , CM000665.1:g.191074892C>T	GRCh37
NC_000003.10:g.192557586C>T	NCBI36
NG_008994.1:g.33019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.65C>T MANE Select	ENSP00000376249.4:p.Ala22Val
ENST00000392456.4:c.65C>T	ENSP00000376250.4:p.Ala22Val
ENST00000392455.7:c.65C>T	ENSP00000376249.3:p.Ala22Val
ENST00000392456.3:c.65C>T	ENSP00000376250.3:p.Ala22Val
NM_174908.3:c.65C>T	NP_777568.1:p.Ala22Val
NM_178335.2:c.65C>T	NP_848018.1:p.Ala22Val
XM_011512460.1:c.65C>T	XP_011510762.1:p.Ala22Val
NM_178335.3:c.65C>T MANE Select	NP_848018.1:p.Ala22Val
NM_174908.4:c.65C>T	NP_777568.1:p.Ala22Val