Canonical Allele Identifier: CA395733484
Gene: ARMC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31462658T>A , CM000678.2:g.31462658T>A GRCh38
NC_000016.9:g.31473979T>A , CM000678.1:g.31473979T>A GRCh37
NC_000016.8:g.31381480T>A NCBI36
NG_034258.1:g.9386T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268314.9:c.1111T>A MANE Select ENSP00000268314.4:p.Leu371Met
ENST00000268314.8:c.1111T>A ENSP00000268314.4:p.Leu371Met
ENST00000408912.7:c.1396T>A ENSP00000386125.3:p.Leu466Met
ENST00000457010.6:c.1111T>A ENSP00000399561.2:p.Leu371Met
ENST00000538189.5:c.619T>A ENSP00000443995.2:p.Leu207Met
ENST00000563544.5:c.1111T>A ENSP00000456877.1:p.Leu371Met
ENST00000564900.1:c.213-114T>A
NM_001105247.1:c.1111T>A NP_001098717.1:p.Leu371Met
NM_001288767.1:c.1396T>A NP_001275696.1:p.Leu466Met
NM_001301820.1:c.1207T>A NP_001288749.1:p.Leu403Met
NM_024742.2:c.1111T>A NP_079018.1:p.Leu371Met
XM_006721091.1:c.1207T>A XP_006721154.1:p.Leu403Met
XM_006721091.3:c.1207T>A XP_006721154.1:p.Leu403Met
XM_024450448.1:c.1207T>A XP_024306216.1:p.Leu403Met
XM_024450449.1:c.1207T>A XP_024306217.1:p.Leu403Met
NM_001105247.2:c.1111T>A MANE Select NP_001098717.1:p.Leu371Met
NM_001288767.2:c.1396T>A NP_001275696.1:p.Leu466Met