Canonical Allele Identifier: CA395732825

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473766G>T (hg19) ; chr16:g.31462445G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462445G>T , CM000678.2:g.31462445G>T	GRCh38
NC_000016.9:g.31473766G>T , CM000678.1:g.31473766G>T	GRCh37
NC_000016.8:g.31381267G>T	NCBI36
NG_034258.1:g.9173G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.898G>T MANE Select	ENSP00000268314.4:p.Gly300Ter
ENST00000268314.8:c.898G>T	ENSP00000268314.4:p.Gly300Ter
ENST00000408912.7:c.1183G>T	ENSP00000386125.3:p.Gly395Ter
ENST00000457010.6:c.898G>T	ENSP00000399561.2:p.Gly300Ter
ENST00000538189.5:c.406G>T	ENSP00000443995.2:p.Gly136Ter
ENST00000563544.5:c.898G>T	ENSP00000456877.1:p.Gly300Ter
ENST00000564900.1:c.212+250G>T
NM_001105247.1:c.898G>T	NP_001098717.1:p.Gly300Ter
NM_001288767.1:c.1183G>T	NP_001275696.1:p.Gly395Ter
NM_001301820.1:c.994G>T	NP_001288749.1:p.Gly332Ter
NM_024742.2:c.898G>T	NP_079018.1:p.Gly300Ter
XM_006721091.1:c.994G>T	XP_006721154.1:p.Gly332Ter
XM_006721091.3:c.994G>T	XP_006721154.1:p.Gly332Ter
XM_024450448.1:c.994G>T	XP_024306216.1:p.Gly332Ter
XM_024450449.1:c.994G>T	XP_024306217.1:p.Gly332Ter
NM_001105247.2:c.898G>T MANE Select	NP_001098717.1:p.Gly300Ter
NM_001288767.2:c.1183G>T	NP_001275696.1:p.Gly395Ter