Canonical Allele Identifier: CA395733170

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473829G>C (hg19) ; chr16:g.31462508G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462508G>C , CM000678.2:g.31462508G>C	GRCh38
NC_000016.9:g.31473829G>C , CM000678.1:g.31473829G>C	GRCh37
NC_000016.8:g.31381330G>C	NCBI36
NG_034258.1:g.9236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.961G>C MANE Select	ENSP00000268314.4:p.Ala321Pro
ENST00000268314.8:c.961G>C	ENSP00000268314.4:p.Ala321Pro
ENST00000408912.7:c.1246G>C	ENSP00000386125.3:p.Ala416Pro
ENST00000457010.6:c.961G>C	ENSP00000399561.2:p.Ala321Pro
ENST00000538189.5:c.469G>C	ENSP00000443995.2:p.Ala157Pro
ENST00000563544.5:c.961G>C	ENSP00000456877.1:p.Ala321Pro
ENST00000564900.1:c.213-264G>C
NM_001105247.1:c.961G>C	NP_001098717.1:p.Ala321Pro
NM_001288767.1:c.1246G>C	NP_001275696.1:p.Ala416Pro
NM_001301820.1:c.1057G>C	NP_001288749.1:p.Ala353Pro
NM_024742.2:c.961G>C	NP_079018.1:p.Ala321Pro
XM_006721091.1:c.1057G>C	XP_006721154.1:p.Ala353Pro
XM_006721091.3:c.1057G>C	XP_006721154.1:p.Ala353Pro
XM_024450448.1:c.1057G>C	XP_024306216.1:p.Ala353Pro
XM_024450449.1:c.1057G>C	XP_024306217.1:p.Ala353Pro
NM_001105247.2:c.961G>C MANE Select	NP_001098717.1:p.Ala321Pro
NM_001288767.2:c.1246G>C	NP_001275696.1:p.Ala416Pro