Canonical Allele Identifier: CA395733459

Gene: ARMC5

Linked Data

• gnomAD v4: 16-31462646-G-T
• COSMIC: COSM3707023 ; COSM3707024
• MyVariant Identifiers: chr16:g.31473967G>T (hg19) ; chr16:g.31462646G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462646G>T , CM000678.2:g.31462646G>T	GRCh38
NC_000016.9:g.31473967G>T , CM000678.1:g.31473967G>T	GRCh37
NC_000016.8:g.31381468G>T	NCBI36
NG_034258.1:g.9374G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1099G>T MANE Select	ENSP00000268314.4:p.Asp367Tyr
ENST00000268314.8:c.1099G>T	ENSP00000268314.4:p.Asp367Tyr
ENST00000408912.7:c.1384G>T	ENSP00000386125.3:p.Asp462Tyr
ENST00000457010.6:c.1099G>T	ENSP00000399561.2:p.Asp367Tyr
ENST00000538189.5:c.607G>T	ENSP00000443995.2:p.Asp203Tyr
ENST00000563544.5:c.1099G>T	ENSP00000456877.1:p.Asp367Tyr
ENST00000564900.1:c.213-126G>T
NM_001105247.1:c.1099G>T	NP_001098717.1:p.Asp367Tyr
NM_001288767.1:c.1384G>T	NP_001275696.1:p.Asp462Tyr
NM_001301820.1:c.1195G>T	NP_001288749.1:p.Asp399Tyr
NM_024742.2:c.1099G>T	NP_079018.1:p.Asp367Tyr
XM_006721091.1:c.1195G>T	XP_006721154.1:p.Asp399Tyr
XM_006721091.3:c.1195G>T	XP_006721154.1:p.Asp399Tyr
XM_024450448.1:c.1195G>T	XP_024306216.1:p.Asp399Tyr
XM_024450449.1:c.1195G>T	XP_024306217.1:p.Asp399Tyr
NM_001105247.2:c.1099G>T MANE Select	NP_001098717.1:p.Asp367Tyr
NM_001288767.2:c.1384G>T	NP_001275696.1:p.Asp462Tyr