Canonical Allele Identifier: CA12442330

Gene: CCDC167

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37483920G>T , CM000668.2:g.37483920G>T	GRCh38
NC_000006.11:g.37451696G>T , CM000668.1:g.37451696G>T	GRCh37
NC_000006.10:g.37559674G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373408.4:c.191-631C>A MANE Select	ENSP00000362507.3:n.191-631C>A
ENST00000373408.3:c.191-631C>A	ENSP00000362507.3:n.191-631C>A
NM_138493.2:c.191-631C>A	NP_612502.1:n.191-631C>A
NM_138493.3:c.191-631C>A MANE Select	NP_612502.1:n.191-631C>A