Canonical Allele Identifier: CA347713533
Gene: CNNM4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761399G>T , CM000664.2:g.96761399G>T GRCh38
NC_000002.11:g.97427136G>T , CM000664.1:g.97427136G>T GRCh37
NC_000002.10:g.96790863G>T NCBI36
NG_016608.1:g.5498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.400G>T MANE Select ENSP00000366275.2:p.Val134Leu
ENST00000377075.2:c.400G>T ENSP00000366275.2:p.Val134Leu
NM_020184.3:c.400G>T NP_064569.3:p.Val134Leu
XM_005263914.2:c.400G>T XP_005263971.1:p.Val134Leu
XM_005263915.2:c.400G>T XP_005263972.1:p.Val134Leu
XM_011510955.1:c.400G>T XP_011509257.1:p.Val134Leu
XM_011510956.1:c.400G>T XP_011509258.1:p.Val134Leu
XM_005263914.4:c.400G>T XP_005263971.1:p.Val134Leu
XM_005263915.4:c.400G>T XP_005263972.1:p.Val134Leu
XM_011510955.3:c.400G>T XP_011509257.1:p.Val134Leu
XM_011510956.3:c.400G>T XP_011509258.1:p.Val134Leu
NM_020184.4:c.400G>T MANE Select NP_064569.3:p.Val134Leu