Canonical Allele Identifier: CA2728845112
Gene: ABCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2139285344

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95061630_95061631insGAAGCAATTTTCAGACTC , CM000675.2:g.95061630_95061631insGAAGCAATTTTCAGACTC GRCh38
NC_000013.10:g.95713884_95713885insGAAGCAATTTTCAGACTC , CM000675.1:g.95713884_95713885insGAAGCAATTTTCAGACTC GRCh37
NC_000013.9:g.94511885_94511886insGAAGCAATTTTCAGACTC NCBI36
NG_050651.1:g.244816_244817insGAGTCTGAAAATTGCTTC
NG_050651.2:g.244816_244817insGAGTCTGAAAATTGCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000643051.1:c.*991+1073_*991+1074insGAGTCTGAAAATTGCTTC ENSP00000495513.1:n.*991+1073_*991+1074insGAGTCTGAAAATTGCTTC
ENST00000643842.1:c.*3412+1073_*3412+1074insGAGTCTGAAAATTGCTTC ENSP00000493861.1:n.*3412+1073_*3412+1074insGAGTCTGAAAATTGCTT...
ENST00000645237.2:c.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC MANE Select ENSP00000494609.1:n.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC
ENST00000646439.1:c.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC ENSP00000494751.1:n.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC
ENST00000376887.8:c.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC ENSP00000366084.4:n.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC
NM_001301829.1:c.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC NP_001288758.1:n.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC
NM_005845.4:c.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC NP_005836.2:n.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC
XM_005254025.2:c.3237+1073_3237+1074insGAGTCTGAAAATTGCTTC XP_005254082.1:n.3237+1073_3237+1074insGAGTCTGAAAATTGCTTC
XM_006719914.1:c.3276+1073_3276+1074insGAGTCTGAAAATTGCTTC XP_006719977.1:n.3276+1073_3276+1074insGAGTCTGAAAATTGCTTC
XM_011521047.1:c.2817+1073_2817+1074insGAGTCTGAAAATTGCTTC XP_011519349.1:n.2817+1073_2817+1074insGAGTCTGAAAATTGCTTC
XM_017020319.1:c.3237+1073_3237+1074insGAGTCTGAAAATTGCTTC XP_016875808.1:n.3237+1073_3237+1074insGAGTCTGAAAATTGCTTC
XM_017020321.1:c.1851+1073_1851+1074insGAGTCTGAAAATTGCTTC XP_016875810.1:n.1851+1073_1851+1074insGAGTCTGAAAATTGCTTC
NM_001301829.2:c.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC NP_001288758.1:n.3225+1073_3225+1074insGAGTCTGAAAATTGCTTC
NM_005845.5:c.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC MANE Select NP_005836.2:n.3366+1073_3366+1074insGAGTCTGAAAATTGCTTC