Canonical Allele Identifier: CA1064142553
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73419727_73419728insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG , CM000666.2:g.73419727_73419728insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG GRCh38
NC_000004.11:g.74285444_74285445insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG , CM000666.1:g.74285444_74285445insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG GRCh37
NC_000004.10:g.74504308_74504309insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG NCBI36
NG_009291.1:g.20473_20474insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG MANE Select ENSP00000295897.4:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTC...
ENST00000295897.8:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000295897.4:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTC...
ENST00000401494.7:c.1440+88_1440+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000384695.3:n.1440+88_1440+89insGATTTATATATACAGTTCTCTTC...
ENST00000415165.6:c.1209+88_1209+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000401820.2:n.1209+88_1209+89insGATTTATATATACAGTTCTCTTC...
ENST00000476441.6:c.*1064+88_*1064+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000423727.1:n.*1064+88_*1064+89insGATTTATATATACAGTTCTCT...
ENST00000495173.1:n.93+88_93+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG
ENST00000503124.5:c.1335+88_1335+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000421027.1:n.1335+88_1335+89insGATTTATATATACAGTTCTCTTC...
ENST00000505649.5:n.1332+88_1332+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG
ENST00000508932.5:n.175+272_175+273insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG
ENST00000509063.5:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000422784.1:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTC...
ENST00000511370.1:c.1318+88_1318+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG
ENST00000621085.4:c.1146+88_1146+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000483421.1:n.1146+88_1146+89insGATTTATATATACAGTTCTCTTC...
ENST00000621628.4:c.1146+88_1146+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG ENSP00000480485.1:n.1146+88_1146+89insGATTTATATATACAGTTCTCTTC...
NM_000477.5:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG NP_000468.1:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTA...
NM_000477.6:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG NP_000468.1:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTA...
NM_000477.7:c.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTAATATGTCCAGTATTCATTTTTGCATGTTTGGTTAGGCTAGGGCTTAGGGATTTATATATCAAAGG MANE Select NP_000468.1:n.1785+88_1785+89insGATTTATATATACAGTTCTCTTCATTTTA...