Canonical Allele Identifier: CA1896422528

Gene: ARMC3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.23014324T= , CM000672.2:g.23014324T=	GRCh38
NC_000010.10:g.23303253T= , CM000672.1:g.23303253T=	GRCh37
NC_000010.9:g.23343259T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173081.5:c.2045+5393T= MANE Select	NP_775104.2:n.2045+5393T=
ENST00000298032.10:c.2045+5393T= MANE Select	ENSP00000298032.5:n.2045+5393T=
NM_001282745.1:c.2024+5393T=	NP_001269674.1:n.2024+5393T=
NM_001282745.2:c.2024+5393T=	NP_001269674.1:n.2024+5393T=
NM_001282746.1:c.*203T=	NP_001269675.1:n.*203T=
NM_001282746.2:c.*203T=	NP_001269675.1:n.*203T=
NM_001282747.1:c.1256+5393T=	NP_001269676.1:n.1256+5393T=
NM_001282747.2:c.1256+5393T=	NP_001269676.1:n.1256+5393T=
NM_173081.4:c.2045+5393T=	NP_775104.2:n.2045+5393T=
ENST00000298032.9:c.2045+5393T=	ENSP00000298032.5:n.2045+5393T=
ENST00000376528.8:c.1256+5393T=	ENSP00000365711.4:n.1256+5393T=
ENST00000409049.7:c.*203T=	ENSP00000387288.3:n.*203T=
ENST00000409983.7:c.2024+5393T=	ENSP00000386943.3:n.2024+5393T=
XM_005252380.1:c.1850+5393T=	XP_005252437.1:n.1850+5393T=
XM_005252380.3:c.1850+5393T=	XP_005252437.1:n.1850+5393T=
XM_005252381.1:c.1781+5393T=	XP_005252438.1:n.1781+5393T=
XM_005252381.2:c.1781+5393T=	XP_005252438.1:n.1781+5393T=
XM_011519350.1:c.2046-2550T=	XP_011517652.1:n.2046-2550T=
XM_011519350.3:c.2046-2550T=	XP_011517652.1:n.2046-2550T=
XM_011519351.1:c.773+5393T=	XP_011517653.1:n.773+5393T=
XM_011519351.2:c.773+5393T=	XP_011517653.1:n.773+5393T=
XM_017015831.2:c.1829+5393T=	XP_016871320.1:n.1829+5393T=
XM_017015832.2:c.*203T=	XP_016871321.1:n.*203T=
XM_017015833.2:c.*203T=	XP_016871322.1:n.*203T=
XR_001747394.1:n.555-18506A=