Canonical Allele Identifier: CA813921386

Linked Data

dbSNP Id: rs1402053901

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74721837_74721841dup , CM000667.2:g.74721837_74721841dup GRCh38
NC_000005.9:g.74017662_74017666dup , CM000667.1:g.74017662_74017666dup GRCh37
NC_000005.8:g.74053418_74053422dup NCBI36
NG_009770.1:g.41694_41698dup
NG_011531.1:g.50380_50384dup
NG_009770.2:g.86815_86819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296805.8:c.2212-55_2212-51dup (GFM2) MANE Select ENSP00000296805.3:n.2212-55_2212-51dup
ENST00000296805.7:c.2212-55_2212-51dup (GFM2) ENSP00000296805.3:n.2212-55_2212-51dup
ENST00000345239.6:c.2071-55_2071-51dup (GFM2) ENSP00000296804.3:n.2071-55_2071-51dup
ENST00000503312.5:c.608+401_608+405dup (HEXB)
ENST00000505859.1:c.255+401_255+405dup (HEXB)
ENST00000509430.5:c.2212-55_2212-51dup (GFM2) ENSP00000427004.1:n.2212-55_2212-51dup
ENST00000513867.1:n.380+401_380+405dup (HEXB)
ENST00000515125.5:n.615-55_615-51dup (GFM2)
NM_001281302.1:c.2308-55_2308-51dup (GFM2) NP_001268231.1:n.2308-55_2308-51dup
NM_032380.4:c.2212-55_2212-51dup (GFM2) NP_115756.2:n.2212-55_2212-51dup
NM_170691.2:c.2071-55_2071-51dup (GFM2) NP_733792.1:n.2071-55_2071-51dup
NR_104006.1:n.2531-55_2531-51dup (GFM2)
XM_006714721.2:c.2077-55_2077-51dup (GFM2) XP_006714784.1:n.2077-55_2077-51dup
XM_011543690.1:c.2212-55_2212-51dup (GFM2) XP_011541992.1:n.2212-55_2212-51dup
XM_017009986.1:c.2212-55_2212-51dup (GFM2) XP_016865475.1:n.2212-55_2212-51dup
XR_002956185.1:n.3498-55_3498-51dup (GFM2)
NM_032380.5:c.2212-55_2212-51dup (GFM2) MANE Select NP_115756.2:n.2212-55_2212-51dup
NM_001281302.2:c.2308-55_2308-51dup (GFM2) NP_001268231.1:n.2308-55_2308-51dup
NM_170691.3:c.2071-55_2071-51dup (GFM2) NP_733792.1:n.2071-55_2071-51dup
NR_104006.2:n.2277-55_2277-51dup (GFM2)