Canonical Allele Identifier: CA395732969

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473794G>C (hg19) ; chr16:g.31462473G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462473G>C , CM000678.2:g.31462473G>C	GRCh38
NC_000016.9:g.31473794G>C , CM000678.1:g.31473794G>C	GRCh37
NC_000016.8:g.31381295G>C	NCBI36
NG_034258.1:g.9201G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.926G>C MANE Select	ENSP00000268314.4:p.Cys309Ser
ENST00000268314.8:c.926G>C	ENSP00000268314.4:p.Cys309Ser
ENST00000408912.7:c.1211G>C	ENSP00000386125.3:p.Cys404Ser
ENST00000457010.6:c.926G>C	ENSP00000399561.2:p.Cys309Ser
ENST00000538189.5:c.434G>C	ENSP00000443995.2:p.Cys145Ser
ENST00000563544.5:c.926G>C	ENSP00000456877.1:p.Cys309Ser
ENST00000564900.1:c.212+278G>C
NM_001105247.1:c.926G>C	NP_001098717.1:p.Cys309Ser
NM_001288767.1:c.1211G>C	NP_001275696.1:p.Cys404Ser
NM_001301820.1:c.1022G>C	NP_001288749.1:p.Cys341Ser
NM_024742.2:c.926G>C	NP_079018.1:p.Cys309Ser
XM_006721091.1:c.1022G>C	XP_006721154.1:p.Cys341Ser
XM_006721091.3:c.1022G>C	XP_006721154.1:p.Cys341Ser
XM_024450448.1:c.1022G>C	XP_024306216.1:p.Cys341Ser
XM_024450449.1:c.1022G>C	XP_024306217.1:p.Cys341Ser
NM_001105247.2:c.926G>C MANE Select	NP_001098717.1:p.Cys309Ser
NM_001288767.2:c.1211G>C	NP_001275696.1:p.Cys404Ser