Canonical Allele Identifier: CA1658313068
Gene: MCM9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118827926_118827929delinsCCTT , CM000668.2:g.118827926_118827929delinsCCTT GRCh38
NC_000006.11:g.119149089_119149092delinsCCTT , CM000668.1:g.119149089_119149092delinsCCTT GRCh37
NC_000006.10:g.119255781_119255784delinsCCTT NCBI36
NG_041822.1:g.112234_112237delinsAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000619706.5:c.1730_1732+1delinsAAGG
ENST00000316316.10:c.1730_1732+1delinsAAGG
ENST00000458674.2:c.207-1065_207-1062delinsAAGG
ENST00000619706.4:c.1730_1732+1delinsAAGG
NM_017696.2:c.1730_1732+1delinsAAGG
NM_001378356.1:c.1730_1732+1delinsAAGG
NM_001378357.1:c.1730_1732+1delinsAAGG
NM_001378359.1:c.1730_1732+1delinsAAGG
NM_001378360.1:c.1730_1732+1delinsAAGG
NM_001378364.1:c.1529-1065_1529-1062delinsAAGG NP_001365293.1:n.1529-1065_1529-1062delinsAAGG
NM_001378366.1:c.1604_1606+1delinsAAGG
NM_001378367.1:c.1532_1534+1delinsAAGG
NM_017696.3:c.1730_1732+1delinsAAGG
NR_165493.1:n.1839_1841+1delinsAAGG