Canonical Allele Identifier: CA1272753132
Gene: CNNM4 HGNC NCBI

Linked Data

dbSNP Id: rs2078761566

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761462_96761463del , CM000664.2:g.96761462_96761463del GRCh38
NC_000002.11:g.97427199_97427200del , CM000664.1:g.97427199_97427200del GRCh37
NC_000002.10:g.96790926_96790927del NCBI36
NG_016608.1:g.5561_5562del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.463_464del MANE Select ENSP00000366275.2:p.Gln155AlafsTer?
ENST00000377075.2:c.463_464del ENSP00000366275.2:p.Gln155AlafsTer?
NM_020184.3:c.463_464del NP_064569.3:p.Gln155AlafsTer?
XM_005263914.2:c.463_464del XP_005263971.1:p.Gln155AlafsTer?
XM_005263915.2:c.463_464del XP_005263972.1:p.Gln155AlafsTer?
XM_011510955.1:c.463_464del XP_011509257.1:p.Gln155AlafsTer?
XM_011510956.1:c.463_464del XP_011509258.1:p.Gln155AlafsTer?
XM_005263914.4:c.463_464del XP_005263971.1:p.Gln155AlafsTer?
XM_005263915.4:c.463_464del XP_005263972.1:p.Gln155AlafsTer?
XM_011510955.3:c.463_464del XP_011509257.1:p.Gln155AlafsTer?
XM_011510956.3:c.463_464del XP_011509258.1:p.Gln155AlafsTer?
NM_020184.4:c.463_464del MANE Select NP_064569.3:p.Gln155AlafsTer?