Canonical Allele Identifier: CA1064138962
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409146_73409147insACAC , CM000666.2:g.73409146_73409147insACAC GRCh38
NC_000004.11:g.74274863_74274864insACAC , CM000666.1:g.74274863_74274864insACAC GRCh37
NC_000004.10:g.74493727_74493728insACAC NCBI36
NG_009291.1:g.9892_9893insACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.483-209_483-208insACAC MANE Select ENSP00000295897.4:n.483-209_483-208insACAC
ENST00000295897.8:c.483-209_483-208insACAC ENSP00000295897.4:n.483-209_483-208insACAC
ENST00000401494.7:c.138-209_138-208insACAC ENSP00000384695.3:n.138-209_138-208insACAC
ENST00000415165.6:c.138-2850_138-2849insACAC ENSP00000401820.2:n.138-2850_138-2849insACAC
ENST00000441319.5:c.489-209_489-208insACAC ENSP00000392541.1:n.489-209_489-208insACAC
ENST00000476441.6:c.80-209_80-208insACAC ENSP00000423727.1:n.80-209_80-208insACAC
ENST00000503124.5:c.33-209_33-208insACAC ENSP00000421027.1:n.33-209_33-208insACAC
ENST00000505649.5:n.169-209_169-208insACAC
ENST00000509063.5:c.483-209_483-208insACAC ENSP00000422784.1:n.483-209_483-208insACAC
ENST00000514786.1:n.452-209_452-208insACAC
ENST00000621085.4:c.483-209_483-208insACAC ENSP00000483421.1:n.483-209_483-208insACAC
ENST00000621628.4:c.486+70_486+71insACAC ENSP00000480485.1:n.486+70_486+71insACAC
NM_000477.5:c.483-209_483-208insACAC NP_000468.1:n.483-209_483-208insACAC
NM_000477.6:c.483-209_483-208insACAC NP_000468.1:n.483-209_483-208insACAC
NM_000477.7:c.483-209_483-208insACAC MANE Select NP_000468.1:n.483-209_483-208insACAC