Canonical Allele Identifier: CA658765798
Gene: CNNM4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761585_96761587del , CM000664.2:g.96761585_96761587del GRCh38
NC_000002.11:g.97427322_97427324del , CM000664.1:g.97427322_97427324del GRCh37
NC_000002.10:g.96791049_96791051del NCBI36
NG_016608.1:g.5684_5686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.586_588del MANE Select ENSP00000366275.2:p.Ser196del
ENST00000377075.2:c.586_588del ENSP00000366275.2:p.Ser196del
NM_020184.3:c.586_588del NP_064569.3:p.Ser196del
XM_005263914.2:c.586_588del XP_005263971.1:p.Ser196del
XM_005263915.2:c.586_588del XP_005263972.1:p.Ser196del
XM_011510955.1:c.586_588del XP_011509257.1:p.Ser196del
XM_011510956.1:c.586_588del XP_011509258.1:p.Ser196del
XM_005263914.4:c.586_588del XP_005263971.1:p.Ser196del
XM_005263915.4:c.586_588del XP_005263972.1:p.Ser196del
XM_011510955.3:c.586_588del XP_011509257.1:p.Ser196del
XM_011510956.3:c.586_588del XP_011509258.1:p.Ser196del
NM_020184.4:c.586_588del MANE Select NP_064569.3:p.Ser196del