Canonical Allele Identifier: CA2535202741
Gene: ABCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95061599_95061609del , CM000675.2:g.95061599_95061609del GRCh38
NC_000013.10:g.95713853_95713863del , CM000675.1:g.95713853_95713863del GRCh37
NC_000013.9:g.94511854_94511864del NCBI36
NG_050651.1:g.244838_244848del
NG_050651.2:g.244838_244848del

Transcript Alleles

HGVS Amino-acid Change
ENST00000643051.1:c.*991+1095_*991+1105del ENSP00000495513.1:n.*991+1095_*991+1105del
ENST00000643842.1:c.*3412+1095_*3412+1105del ENSP00000493861.1:n.*3412+1095_*3412+1105del
ENST00000645237.2:c.3366+1095_3366+1105del MANE Select ENSP00000494609.1:n.3366+1095_3366+1105del
ENST00000646439.1:c.3225+1095_3225+1105del ENSP00000494751.1:n.3225+1095_3225+1105del
ENST00000376887.8:c.3366+1095_3366+1105del ENSP00000366084.4:n.3366+1095_3366+1105del
NM_001301829.1:c.3225+1095_3225+1105del NP_001288758.1:n.3225+1095_3225+1105del
NM_005845.4:c.3366+1095_3366+1105del NP_005836.2:n.3366+1095_3366+1105del
XM_005254025.2:c.3237+1095_3237+1105del XP_005254082.1:n.3237+1095_3237+1105del
XM_006719914.1:c.3276+1095_3276+1105del XP_006719977.1:n.3276+1095_3276+1105del
XM_011521047.1:c.2817+1095_2817+1105del XP_011519349.1:n.2817+1095_2817+1105del
XM_017020319.1:c.3237+1095_3237+1105del XP_016875808.1:n.3237+1095_3237+1105del
XM_017020321.1:c.1851+1095_1851+1105del XP_016875810.1:n.1851+1095_1851+1105del
NM_001301829.2:c.3225+1095_3225+1105del NP_001288758.1:n.3225+1095_3225+1105del
NM_005845.5:c.3366+1095_3366+1105del MANE Select NP_005836.2:n.3366+1095_3366+1105del