Canonical Allele Identifier: CA347713628
Gene: CNNM4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761411T>C , CM000664.2:g.96761411T>C GRCh38
NC_000002.11:g.97427148T>C , CM000664.1:g.97427148T>C GRCh37
NC_000002.10:g.96790875T>C NCBI36
NG_016608.1:g.5510T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.412T>C MANE Select ENSP00000366275.2:p.Phe138Leu
ENST00000377075.2:c.412T>C ENSP00000366275.2:p.Phe138Leu
NM_020184.3:c.412T>C NP_064569.3:p.Phe138Leu
XM_005263914.2:c.412T>C XP_005263971.1:p.Phe138Leu
XM_005263915.2:c.412T>C XP_005263972.1:p.Phe138Leu
XM_011510955.1:c.412T>C XP_011509257.1:p.Phe138Leu
XM_011510956.1:c.412T>C XP_011509258.1:p.Phe138Leu
XM_005263914.4:c.412T>C XP_005263971.1:p.Phe138Leu
XM_005263915.4:c.412T>C XP_005263972.1:p.Phe138Leu
XM_011510955.3:c.412T>C XP_011509257.1:p.Phe138Leu
XM_011510956.3:c.412T>C XP_011509258.1:p.Phe138Leu
NM_020184.4:c.412T>C MANE Select NP_064569.3:p.Phe138Leu