Canonical Allele Identifier: CA1468152569
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718805651

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409164_73409165insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT , CM000666.2:g.73409164_73409165insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT GRCh38
NC_000004.11:g.74274881_74274882insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT , CM000666.1:g.74274881_74274882insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT GRCh37
NC_000004.10:g.74493745_74493746insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT NCBI36
NG_009291.1:g.9910_9911insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT MANE Select ENSP00000295897.4:n.483-191_483-190insCAGTTATACATCCATGTTTGTAA...
ENST00000295897.8:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000295897.4:n.483-191_483-190insCAGTTATACATCCATGTTTGTAA...
ENST00000401494.7:c.138-191_138-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000384695.3:n.138-191_138-190insCAGTTATACATCCATGTTTGTAA...
ENST00000415165.6:c.138-2832_138-2831insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000401820.2:n.138-2832_138-2831insCAGTTATACATCCATGTTTGT...
ENST00000441319.5:c.489-191_489-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000392541.1:n.489-191_489-190insCAGTTATACATCCATGTTTGTAA...
ENST00000476441.6:c.80-191_80-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000423727.1:n.80-191_80-190insCAGTTATACATCCATGTTTGTAAAC...
ENST00000503124.5:c.33-191_33-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000421027.1:n.33-191_33-190insCAGTTATACATCCATGTTTGTAAAC...
ENST00000505649.5:n.169-191_169-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT
ENST00000509063.5:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000422784.1:n.483-191_483-190insCAGTTATACATCCATGTTTGTAA...
ENST00000514786.1:n.452-191_452-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT
ENST00000621085.4:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000483421.1:n.483-191_483-190insCAGTTATACATCCATGTTTGTAA...
ENST00000621628.4:c.486+88_486+89insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT ENSP00000480485.1:n.486+88_486+89insCAGTTATACATCCATGTTTGTAAAC...
NM_000477.5:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT NP_000468.1:n.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCT...
NM_000477.6:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT NP_000468.1:n.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCT...
NM_000477.7:c.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCTTAGTCAGT MANE Select NP_000468.1:n.483-191_483-190insCAGTTATACATCCATGTTTGTAAACTTCT...