Canonical Allele Identifier: CA347713771
Gene: CNNM4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761433T>G , CM000664.2:g.96761433T>G GRCh38
NC_000002.11:g.97427170T>G , CM000664.1:g.97427170T>G GRCh37
NC_000002.10:g.96790897T>G NCBI36
NG_016608.1:g.5532T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.434T>G MANE Select ENSP00000366275.2:p.Met145Arg
ENST00000377075.2:c.434T>G ENSP00000366275.2:p.Met145Arg
NM_020184.3:c.434T>G NP_064569.3:p.Met145Arg
XM_005263914.2:c.434T>G XP_005263971.1:p.Met145Arg
XM_005263915.2:c.434T>G XP_005263972.1:p.Met145Arg
XM_011510955.1:c.434T>G XP_011509257.1:p.Met145Arg
XM_011510956.1:c.434T>G XP_011509258.1:p.Met145Arg
XM_005263914.4:c.434T>G XP_005263971.1:p.Met145Arg
XM_005263915.4:c.434T>G XP_005263972.1:p.Met145Arg
XM_011510955.3:c.434T>G XP_011509257.1:p.Met145Arg
XM_011510956.3:c.434T>G XP_011509258.1:p.Met145Arg
NM_020184.4:c.434T>G MANE Select NP_064569.3:p.Met145Arg