Canonical Allele Identifier: CA1064138979
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs55764359

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409165_73409172del , CM000666.2:g.73409165_73409172del GRCh38
NC_000004.11:g.74274882_74274889del , CM000666.1:g.74274882_74274889del GRCh37
NC_000004.10:g.74493746_74493753del NCBI36
NG_009291.1:g.9911_9918del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.483-190_483-183del MANE Select ENSP00000295897.4:n.483-190_483-183del
ENST00000295897.8:c.483-190_483-183del ENSP00000295897.4:n.483-190_483-183del
ENST00000401494.7:c.138-190_138-183del ENSP00000384695.3:n.138-190_138-183del
ENST00000415165.6:c.138-2831_138-2824del ENSP00000401820.2:n.138-2831_138-2824del
ENST00000441319.5:c.489-190_489-183del ENSP00000392541.1:n.489-190_489-183del
ENST00000476441.6:c.80-190_80-183del ENSP00000423727.1:n.80-190_80-183del
ENST00000503124.5:c.33-190_33-183del ENSP00000421027.1:n.33-190_33-183del
ENST00000505649.5:n.169-190_169-183del
ENST00000509063.5:c.483-190_483-183del ENSP00000422784.1:n.483-190_483-183del
ENST00000514786.1:n.452-190_452-183del
ENST00000621085.4:c.483-190_483-183del ENSP00000483421.1:n.483-190_483-183del
ENST00000621628.4:c.486+89_486+96del ENSP00000480485.1:n.486+89_486+96del
NM_000477.5:c.483-190_483-183del NP_000468.1:n.483-190_483-183del
NM_000477.6:c.483-190_483-183del NP_000468.1:n.483-190_483-183del
NM_000477.7:c.483-190_483-183del MANE Select NP_000468.1:n.483-190_483-183del