Canonical Allele Identifier: CA395733436
Gene: ARMC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31462631C>G , CM000678.2:g.31462631C>G GRCh38
NC_000016.9:g.31473952C>G , CM000678.1:g.31473952C>G GRCh37
NC_000016.8:g.31381453C>G NCBI36
NG_034258.1:g.9359C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268314.9:c.1084C>G MANE Select ENSP00000268314.4:p.Arg362Gly
ENST00000268314.8:c.1084C>G ENSP00000268314.4:p.Arg362Gly
ENST00000408912.7:c.1369C>G ENSP00000386125.3:p.Arg457Gly
ENST00000457010.6:c.1084C>G ENSP00000399561.2:p.Arg362Gly
ENST00000538189.5:c.592C>G ENSP00000443995.2:p.Arg198Gly
ENST00000563544.5:c.1084C>G ENSP00000456877.1:p.Arg362Gly
ENST00000564900.1:c.213-141C>G
NM_001105247.1:c.1084C>G NP_001098717.1:p.Arg362Gly
NM_001288767.1:c.1369C>G NP_001275696.1:p.Arg457Gly
NM_001301820.1:c.1180C>G NP_001288749.1:p.Arg394Gly
NM_024742.2:c.1084C>G NP_079018.1:p.Arg362Gly
XM_006721091.1:c.1180C>G XP_006721154.1:p.Arg394Gly
XM_006721091.3:c.1180C>G XP_006721154.1:p.Arg394Gly
XM_024450448.1:c.1180C>G XP_024306216.1:p.Arg394Gly
XM_024450449.1:c.1180C>G XP_024306217.1:p.Arg394Gly
NM_001105247.2:c.1084C>G MANE Select NP_001098717.1:p.Arg362Gly
NM_001288767.2:c.1369C>G NP_001275696.1:p.Arg457Gly