Canonical Allele Identifier: CA2669071447

Gene: CCDC50

Linked Data

• gnomAD v4: 3-191356979-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191356979G>T , CM000665.2:g.191356979G>T	GRCh38
NC_000003.11:g.191074768G>T , CM000665.1:g.191074768G>T	GRCh37
NC_000003.10:g.192557462G>T	NCBI36
NG_008994.1:g.32895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.50-109G>T MANE Select	ENSP00000376249.4:n.50-109G>T
ENST00000392456.4:c.50-109G>T	ENSP00000376250.4:n.50-109G>T
ENST00000392455.7:c.50-109G>T	ENSP00000376249.3:n.50-109G>T
ENST00000392456.3:c.50-109G>T	ENSP00000376250.3:n.50-109G>T
NM_174908.3:c.50-109G>T	NP_777568.1:n.50-109G>T
NM_178335.2:c.50-109G>T	NP_848018.1:n.50-109G>T
XM_011512460.1:c.50-109G>T	XP_011510762.1:n.50-109G>T
NM_178335.3:c.50-109G>T MANE Select	NP_848018.1:n.50-109G>T
NM_174908.4:c.50-109G>T	NP_777568.1:n.50-109G>T