Canonical Allele Identifier: CA2670966782
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420321_73420322insCCTACCAT , CM000666.2:g.73420321_73420322insCCTACCAT GRCh38
NC_000004.11:g.74286038_74286039insCCTACCAT , CM000666.1:g.74286038_74286039insCCTACCAT GRCh37
NC_000004.10:g.74504902_74504903insCCTACCAT NCBI36
NG_009291.1:g.21067_21068insCCTACCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.*23_*23+1insCCTACCAT MANE Select ENSP00000295897.4:n.*23_*23+1insCCTACCAT
ENST00000295897.8:c.*23_*23+1insCCTACCAT ENSP00000295897.4:n.*23_*23+1insCCTACCAT
ENST00000401494.7:c.*23_*23+1insCCTACCAT ENSP00000384695.3:n.*23_*23+1insCCTACCAT
ENST00000415165.6:c.*23_*23+1insCCTACCAT ENSP00000401820.2:n.*23_*23+1insCCTACCAT
ENST00000476441.6:c.*1132_*1132+1insCCTACCAT ENSP00000423727.1:n.*1132_*1132+1insCCTACCAT
ENST00000495173.1:n.161_161+1insCCTACCAT
ENST00000503124.5:c.*23_*23+1insCCTACCAT ENSP00000421027.1:n.*23_*23+1insCCTACCAT
ENST00000505649.5:n.1400_1400+1insCCTACCAT
ENST00000508932.5:n.243_243+1insCCTACCAT
ENST00000509063.5:c.1785+682_1785+683insCCTACCAT ENSP00000422784.1:n.1785+682_1785+683insCCTACCAT
ENST00000511370.1:c.1386_1386+1insCCTACCAT
ENST00000621085.4:c.*23_*23+1insCCTACCAT ENSP00000483421.1:n.*23_*23+1insCCTACCAT
ENST00000621628.4:c.*23_*23+1insCCTACCAT ENSP00000480485.1:n.*23_*23+1insCCTACCAT
NM_000477.5:c.*23_*23+1insCCTACCAT NP_000468.1:n.*23_*23+1insCCTACCAT
NM_000477.6:c.*23_*23+1insCCTACCAT NP_000468.1:n.*23_*23+1insCCTACCAT
NM_000477.7:c.*23_*23+1insCCTACCAT MANE Select NP_000468.1:n.*23_*23+1insCCTACCAT