Canonical Allele Identifier: CA1468148764
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420210_73420211delinsTA , CM000666.2:g.73420210_73420211delinsTA GRCh38
NC_000004.11:g.74285927_74285928delinsTA , CM000666.1:g.74285927_74285928delinsTA GRCh37
NC_000004.10:g.74504791_74504792delinsTA NCBI36
NG_009291.1:g.20956_20957delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1786-44_1786-43delinsTA MANE Select ENSP00000295897.4:n.1786-44_1786-43delinsTA
ENST00000295897.8:c.1786-44_1786-43delinsTA ENSP00000295897.4:n.1786-44_1786-43delinsTA
ENST00000401494.7:c.1441-44_1441-43delinsTA ENSP00000384695.3:n.1441-44_1441-43delinsTA
ENST00000415165.6:c.1210-44_1210-43delinsTA ENSP00000401820.2:n.1210-44_1210-43delinsTA
ENST00000476441.6:c.*1065-44_*1065-43delinsTA ENSP00000423727.1:n.*1065-44_*1065-43delinsTA
ENST00000495173.1:n.94-44_94-43delinsTA
ENST00000503124.5:c.1336-44_1336-43delinsTA ENSP00000421027.1:n.1336-44_1336-43delinsTA
ENST00000505649.5:n.1333-44_1333-43delinsTA
ENST00000508932.5:n.176-44_176-43delinsTA
ENST00000509063.5:c.1785+571_1785+572delinsTA ENSP00000422784.1:n.1785+571_1785+572delinsTA
ENST00000511370.1:c.1319-44_1319-43delinsTA
ENST00000621085.4:c.1147-44_1147-43delinsTA ENSP00000483421.1:n.1147-44_1147-43delinsTA
ENST00000621628.4:c.1147-44_1147-43delinsTA ENSP00000480485.1:n.1147-44_1147-43delinsTA
NM_000477.5:c.1786-44_1786-43delinsTA NP_000468.1:n.1786-44_1786-43delinsTA
NM_000477.6:c.1786-44_1786-43delinsTA NP_000468.1:n.1786-44_1786-43delinsTA
NM_000477.7:c.1786-44_1786-43delinsTA MANE Select NP_000468.1:n.1786-44_1786-43delinsTA