Canonical Allele Identifier: CA1468148781
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420228_73420230delinsAAC , CM000666.2:g.73420228_73420230delinsAAC GRCh38
NC_000004.11:g.74285945_74285947delinsAAC , CM000666.1:g.74285945_74285947delinsAAC GRCh37
NC_000004.10:g.74504809_74504811delinsAAC NCBI36
NG_009291.1:g.20974_20976delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1786-26_1786-24delinsAAC MANE Select ENSP00000295897.4:n.1786-26_1786-24delinsAAC
ENST00000295897.8:c.1786-26_1786-24delinsAAC ENSP00000295897.4:n.1786-26_1786-24delinsAAC
ENST00000401494.7:c.1441-26_1441-24delinsAAC ENSP00000384695.3:n.1441-26_1441-24delinsAAC
ENST00000415165.6:c.1210-26_1210-24delinsAAC ENSP00000401820.2:n.1210-26_1210-24delinsAAC
ENST00000476441.6:c.*1065-26_*1065-24delinsAAC ENSP00000423727.1:n.*1065-26_*1065-24delinsAAC
ENST00000495173.1:n.94-26_94-24delinsAAC
ENST00000503124.5:c.1336-26_1336-24delinsAAC ENSP00000421027.1:n.1336-26_1336-24delinsAAC
ENST00000505649.5:n.1333-26_1333-24delinsAAC
ENST00000508932.5:n.176-26_176-24delinsAAC
ENST00000509063.5:c.1785+589_1785+591delinsAAC ENSP00000422784.1:n.1785+589_1785+591delinsAAC
ENST00000511370.1:c.1319-26_1319-24delinsAAC
ENST00000621085.4:c.1147-26_1147-24delinsAAC ENSP00000483421.1:n.1147-26_1147-24delinsAAC
ENST00000621628.4:c.1147-26_1147-24delinsAAC ENSP00000480485.1:n.1147-26_1147-24delinsAAC
NM_000477.5:c.1786-26_1786-24delinsAAC NP_000468.1:n.1786-26_1786-24delinsAAC
NM_000477.6:c.1786-26_1786-24delinsAAC NP_000468.1:n.1786-26_1786-24delinsAAC
NM_000477.7:c.1786-26_1786-24delinsAAC MANE Select NP_000468.1:n.1786-26_1786-24delinsAAC