Canonical Allele Identifier: CA8029599

Gene: ARMC5

Linked Data

• ClinVar Variation Id: 743683
• ClinVar RCV Id: RCV000920055
• dbSNP Id: rs374639681
• ExAC: 16:31473937 C / T
• gnomAD v2: 16-31473937-C-T
• gnomAD v3: 16-31462616-C-T
• gnomAD v4: 16-31462616-C-T
• MyVariant Identifiers: chr16:g.31473937C>T (hg19) ; chr16:g.31462616C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462616C>T , CM000678.2:g.31462616C>T	GRCh38
NC_000016.9:g.31473937C>T , CM000678.1:g.31473937C>T	GRCh37
NC_000016.8:g.31381438C>T	NCBI36
NG_034258.1:g.9344C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1069C>T MANE Select	ENSP00000268314.4:p.Arg357Cys
ENST00000268314.8:c.1069C>T	ENSP00000268314.4:p.Arg357Cys
ENST00000408912.7:c.1354C>T	ENSP00000386125.3:p.Arg452Cys
ENST00000457010.6:c.1069C>T	ENSP00000399561.2:p.Arg357Cys
ENST00000538189.5:c.577C>T	ENSP00000443995.2:p.Arg193Cys
ENST00000563544.5:c.1069C>T	ENSP00000456877.1:p.Arg357Cys
ENST00000564900.1:c.213-156C>T
NM_001105247.1:c.1069C>T	NP_001098717.1:p.Arg357Cys
NM_001288767.1:c.1354C>T	NP_001275696.1:p.Arg452Cys
NM_001301820.1:c.1165C>T	NP_001288749.1:p.Arg389Cys
NM_024742.2:c.1069C>T	NP_079018.1:p.Arg357Cys
XM_006721091.1:c.1165C>T	XP_006721154.1:p.Arg389Cys
XM_006721091.3:c.1165C>T	XP_006721154.1:p.Arg389Cys
XM_024450448.1:c.1165C>T	XP_024306216.1:p.Arg389Cys
XM_024450449.1:c.1165C>T	XP_024306217.1:p.Arg389Cys
NM_001105247.2:c.1069C>T MANE Select	NP_001098717.1:p.Arg357Cys
NM_001288767.2:c.1354C>T	NP_001275696.1:p.Arg452Cys