Canonical Allele Identifier: CA347713763
Gene: CNNM4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.434T>A MANE Select ENSP00000366275.2:p.Met145Lys
ENST00000377075.2:c.434T>A ENSP00000366275.2:p.Met145Lys
NM_020184.3:c.434T>A NP_064569.3:p.Met145Lys
XM_005263914.2:c.434T>A XP_005263971.1:p.Met145Lys
XM_005263915.2:c.434T>A XP_005263972.1:p.Met145Lys
XM_011510955.1:c.434T>A XP_011509257.1:p.Met145Lys
XM_011510956.1:c.434T>A XP_011509258.1:p.Met145Lys
XM_005263914.4:c.434T>A XP_005263971.1:p.Met145Lys
XM_005263915.4:c.434T>A XP_005263972.1:p.Met145Lys
XM_011510955.3:c.434T>A XP_011509257.1:p.Met145Lys
XM_011510956.3:c.434T>A XP_011509258.1:p.Met145Lys
NM_020184.4:c.434T>A MANE Select NP_064569.3:p.Met145Lys