Canonical Allele Identifier: CA1547803859

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56142890_56142891delinsGA , CM000667.2:g.56142890_56142891delinsGA	GRCh38
NC_000005.9:g.55438717_55438718delinsGA , CM000667.1:g.55438717_55438718delinsGA	GRCh37
NC_000005.8:g.55474474_55474475delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341048.9:c.612+910_612+911delinsTC MANE Select	ENSP00000342295.4:n.612+910_612+911delinsTC
ENST00000341048.8:c.612+910_612+911delinsTC	ENSP00000342295.4:n.612+910_612+911delinsTC
ENST00000504958.6:c.484-15785_484-15784delinsTC	ENSP00000424230.1:n.484-15785_484-15784delinsTC
ENST00000505970.2:n.382+910_382+911delinsTC
NM_024669.2:c.612+910_612+911delinsTC	NP_078945.2:n.612+910_612+911delinsTC
XM_006714691.2:c.126+910_126+911delinsTC	XP_006714754.1:n.126+910_126+911delinsTC
XM_011543646.1:c.-65+910_-65+911delinsTC	XP_011541948.1:n.-65+910_-65+911delinsTC
XM_017009852.1:c.612+910_612+911delinsTC	XP_016865341.1:n.612+910_612+911delinsTC
XM_017009853.1:c.612+910_612+911delinsTC	XP_016865342.1:n.612+910_612+911delinsTC
XM_017009854.1:c.126+910_126+911delinsTC	XP_016865343.1:n.126+910_126+911delinsTC
NM_024669.3:c.612+910_612+911delinsTC MANE Select	NP_078945.2:n.612+910_612+911delinsTC