Canonical Allele Identifier: CA1783323

Gene: CNNM4

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96762311dup , CM000664.2:g.96762311dup	GRCh38
NC_000002.11:g.97428048dup , CM000664.1:g.97428048dup	GRCh37
NC_000002.10:g.96791775dup	NCBI36
NG_016608.1:g.6410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.1312dup MANE Select	ENSP00000366275.2:p.Leu438ProfsTer9
ENST00000377075.2:c.1312dup	ENSP00000366275.2:p.Leu438ProfsTer9
NM_020184.3:c.1312dup	NP_064569.3:p.Leu438ProfsTer9
XM_005263914.2:c.1312dup	XP_005263971.1:p.Leu438ProfsTer9
XM_005263915.2:c.1312dup	XP_005263972.1:p.Leu438ProfsTer9
XM_011510955.1:c.1312dup	XP_011509257.1:p.Leu438ProfsTer9
XM_011510956.1:c.1312dup	XP_011509258.1:p.Leu438ProfsTer9
XM_005263914.4:c.1312dup	XP_005263971.1:p.Leu438ProfsTer9
XM_005263915.4:c.1312dup	XP_005263972.1:p.Leu438ProfsTer9
XM_011510955.3:c.1312dup	XP_011509257.1:p.Leu438ProfsTer9
XM_011510956.3:c.1312dup	XP_011509258.1:p.Leu438ProfsTer9
NM_020184.4:c.1312dup MANE Select	NP_064569.3:p.Leu438ProfsTer9