Canonical Allele Identifier: CA2660221302

Gene: CNNM4

Linked Data

• gnomAD v4: 2-96761453-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761456del , CM000664.2:g.96761456del	GRCh38
NC_000002.11:g.97427193del , CM000664.1:g.97427193del	GRCh37
NC_000002.10:g.96790920del	NCBI36
NG_016608.1:g.5555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.457del MANE Select	ENSP00000366275.2:p.Arg153GlyfsTer9
ENST00000377075.2:c.457del	ENSP00000366275.2:p.Arg153GlyfsTer9
NM_020184.3:c.457del	NP_064569.3:p.Arg153GlyfsTer9
XM_005263914.2:c.457del	XP_005263971.1:p.Arg153GlyfsTer9
XM_005263915.2:c.457del	XP_005263972.1:p.Arg153GlyfsTer9
XM_011510955.1:c.457del	XP_011509257.1:p.Arg153GlyfsTer9
XM_011510956.1:c.457del	XP_011509258.1:p.Arg153GlyfsTer9
XM_005263914.4:c.457del	XP_005263971.1:p.Arg153GlyfsTer9
XM_005263915.4:c.457del	XP_005263972.1:p.Arg153GlyfsTer9
XM_011510955.3:c.457del	XP_011509257.1:p.Arg153GlyfsTer9
XM_011510956.3:c.457del	XP_011509258.1:p.Arg153GlyfsTer9
NM_020184.4:c.457del MANE Select	NP_064569.3:p.Arg153GlyfsTer9