Canonical Allele Identifier: CA8029446

Gene: ARMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31459963A>G , CM000678.2:g.31459963A>G	GRCh38
NC_000016.9:g.31471284A>G , CM000678.1:g.31471284A>G	GRCh37
NC_000016.8:g.31378785A>G	NCBI36
NG_034258.1:g.6691A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001105247.2:c.439A>G MANE Select	NP_001098717.1:p.Thr147Ala
ENST00000268314.9:c.439A>G MANE Select	ENSP00000268314.4:p.Thr147Ala
NM_001105247.1:c.439A>G	NP_001098717.1:p.Thr147Ala
NM_001288767.1:c.724A>G	NP_001275696.1:p.Thr242Ala
NM_001288767.2:c.724A>G	NP_001275696.1:p.Thr242Ala
NM_001301820.1:c.535A>G	NP_001288749.1:p.Thr179Ala
NM_024742.2:c.439A>G	NP_079018.1:p.Thr147Ala
ENST00000268314.8:c.439A>G	ENSP00000268314.4:p.Thr147Ala
ENST00000408912.7:c.724A>G	ENSP00000386125.3:p.Thr242Ala
ENST00000457010.6:c.439A>G	ENSP00000399561.2:p.Thr147Ala
ENST00000538189.5:c.-54A>G	ENSP00000443995.2:n.-54A>G
ENST00000563544.5:c.439A>G	ENSP00000456877.1:p.Thr147Ala
ENST00000564900.1:c.3A>G
XM_006721091.1:c.535A>G	XP_006721154.1:p.Thr179Ala
XM_006721091.3:c.535A>G	XP_006721154.1:p.Thr179Ala
XM_024450448.1:c.535A>G	XP_024306216.1:p.Thr179Ala
XM_024450449.1:c.535A>G	XP_024306217.1:p.Thr179Ala