Canonical Allele Identifier: CA13147461
Gene: ARMC3 HGNC NCBI

Linked Data

dbSNP Id: rs1054052
gnomAD v2: 10-23303253-T-A
gnomAD v3: 10-23014324-T-A
gnomAD v4: 10-23014324-T-A
MyVariant Identifiers: chr10:g.23303253T>A (hg19) chr10:g.23014324T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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