Canonical Allele Identifier: CA2838256101
Gene: ARK2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46404079T>C , CM000680.2:g.46404079T>C GRCh38
NC_000018.9:g.43984042T>C , CM000680.1:g.43984042T>C GRCh37
NC_000018.8:g.42238040T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269439.12:c.62-29111T>C MANE Select ENSP00000269439.6:n.62-29111T>C
ENST00000269439.11:c.62-29111T>C ENSP00000269439.6:n.62-29111T>C
ENST00000543885.2:c.-91-43484T>C ENSP00000444285.1:n.-91-43484T>C
ENST00000586604.5:c.62-43484T>C ENSP00000468365.1:n.62-43484T>C
ENST00000593230.5:c.-140-29111T>C ENSP00000467730.1:n.-140-29111T>C
NM_001256758.1:c.-91-43484T>C NP_001243687.1:n.-91-43484T>C
NM_152470.2:c.62-29111T>C NP_689683.2:n.62-29111T>C
XM_011526016.1:c.62-29111T>C XP_011524318.1:n.62-29111T>C
XM_011526017.1:c.62-29111T>C XP_011524319.1:n.62-29111T>C
XM_011526016.3:c.62-29111T>C XP_011524318.1:n.62-29111T>C
XM_017025788.2:c.62-29111T>C XP_016881277.1:n.62-29111T>C
NM_152470.3:c.62-29111T>C MANE Select NP_689683.2:n.62-29111T>C