Canonical Allele Identifier: CA1468149108
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420513_73420516delinsAGAT , CM000666.2:g.73420513_73420516delinsAGAT GRCh38
NC_000004.11:g.74286230_74286233delinsAGAT , CM000666.1:g.74286230_74286233delinsAGAT GRCh37
NC_000004.10:g.74505094_74505097delinsAGAT NCBI36
NG_009291.1:g.21259_21262delinsAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.*23+192_*23+195delinsAGAT MANE Select ENSP00000295897.4:n.*23+192_*23+195delinsAGAT
ENST00000295897.8:c.*23+192_*23+195delinsAGAT ENSP00000295897.4:n.*23+192_*23+195delinsAGAT
ENST00000401494.7:c.*23+192_*23+195delinsAGAT ENSP00000384695.3:n.*23+192_*23+195delinsAGAT
ENST00000415165.6:c.*23+192_*23+195delinsAGAT ENSP00000401820.2:n.*23+192_*23+195delinsAGAT
ENST00000476441.6:c.*1132+192_*1132+195delinsAGAT ENSP00000423727.1:n.*1132+192_*1132+195delinsAGAT
ENST00000495173.1:n.161+192_161+195delinsAGAT
ENST00000503124.5:c.*23+192_*23+195delinsAGAT ENSP00000421027.1:n.*23+192_*23+195delinsAGAT
ENST00000505649.5:n.1400+192_1400+195delinsAGAT
ENST00000508932.5:n.243+192_243+195delinsAGAT
ENST00000509063.5:c.1786-579_1786-576delinsAGAT ENSP00000422784.1:n.1786-579_1786-576delinsAGAT
ENST00000511370.1:c.1386+192_1386+195delinsAGAT
ENST00000621085.4:c.*23+192_*23+195delinsAGAT ENSP00000483421.1:n.*23+192_*23+195delinsAGAT
ENST00000621628.4:c.*23+192_*23+195delinsAGAT ENSP00000480485.1:n.*23+192_*23+195delinsAGAT
NM_000477.5:c.*23+192_*23+195delinsAGAT NP_000468.1:n.*23+192_*23+195delinsAGAT
NM_000477.6:c.*23+192_*23+195delinsAGAT NP_000468.1:n.*23+192_*23+195delinsAGAT
NM_000477.7:c.*23+192_*23+195delinsAGAT MANE Select NP_000468.1:n.*23+192_*23+195delinsAGAT