Canonical Allele Identifier: CA355764231

Gene: CCDC50

Linked Data

• MyVariant Identifiers: chr3:g.191093070A>T (hg19) ; chr3:g.191375281A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375281A>T , CM000665.2:g.191375281A>T	GRCh38
NC_000003.11:g.191093070A>T , CM000665.1:g.191093070A>T	GRCh37
NC_000003.10:g.192575764A>T	NCBI36
NG_008994.1:g.51197A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.668A>T MANE Select	ENSP00000376249.4:p.His223Leu
ENST00000392456.4:c.449-4878A>T	ENSP00000376250.4:n.449-4878A>T
ENST00000392455.7:c.449-4878A>T	ENSP00000376249.3:n.449-4878A>T
ENST00000392456.3:c.668A>T	ENSP00000376250.3:p.His223Leu
NM_174908.3:c.449-4878A>T	NP_777568.1:n.449-4878A>T
NM_178335.2:c.668A>T	NP_848018.1:p.His223Leu
XM_011512460.1:c.668A>T	XP_011510762.1:p.His223Leu
NM_178335.3:c.668A>T MANE Select	NP_848018.1:p.His223Leu
NM_174908.4:c.449-4878A>T	NP_777568.1:n.449-4878A>T