Canonical Allele Identifier: CA1547803848

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56142875_56142876delinsTG , CM000667.2:g.56142875_56142876delinsTG	GRCh38
NC_000005.9:g.55438702_55438703delinsTG , CM000667.1:g.55438702_55438703delinsTG	GRCh37
NC_000005.8:g.55474459_55474460delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341048.9:c.612+925_612+926delinsCA MANE Select	ENSP00000342295.4:n.612+925_612+926delinsCA
ENST00000341048.8:c.612+925_612+926delinsCA	ENSP00000342295.4:n.612+925_612+926delinsCA
ENST00000504958.6:c.484-15770_484-15769delinsCA	ENSP00000424230.1:n.484-15770_484-15769delinsCA
ENST00000505970.2:n.382+925_382+926delinsCA
NM_024669.2:c.612+925_612+926delinsCA	NP_078945.2:n.612+925_612+926delinsCA
XM_006714691.2:c.126+925_126+926delinsCA	XP_006714754.1:n.126+925_126+926delinsCA
XM_011543646.1:c.-65+925_-65+926delinsCA	XP_011541948.1:n.-65+925_-65+926delinsCA
XM_017009852.1:c.612+925_612+926delinsCA	XP_016865341.1:n.612+925_612+926delinsCA
XM_017009853.1:c.612+925_612+926delinsCA	XP_016865342.1:n.612+925_612+926delinsCA
XM_017009854.1:c.126+925_126+926delinsCA	XP_016865343.1:n.126+925_126+926delinsCA
NM_024669.3:c.612+925_612+926delinsCA MANE Select	NP_078945.2:n.612+925_612+926delinsCA