Canonical Allele Identifier: CA2578063688
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404329del , CM000666.2:g.73404329del GRCh38
NC_000004.11:g.74270046del , CM000666.1:g.74270046del GRCh37
NC_000004.10:g.74488910del NCBI36
NG_009291.1:g.5075del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.2del MANE Select ENSP00000295897.4:p.Met1ArgfsTer4
ENST00000295897.8:c.2del ENSP00000295897.4:p.Met1ArgfsTer4
ENST00000401494.7:c.2del ENSP00000384695.3:p.Met1ArgfsTer4
ENST00000415165.6:c.2del ENSP00000401820.2:p.Met1ArgfsTer4
ENST00000441319.5:c.48-40del ENSP00000392541.1:n.48-40del
ENST00000476441.6:c.2del ENSP00000423727.1:p.Met1ArgfsTer4
ENST00000503124.5:c.-179del ENSP00000421027.1:n.-179del
ENST00000509063.5:c.2del ENSP00000422784.1:p.Met1ArgfsTer4
ENST00000510166.5:n.43del
ENST00000514786.1:n.41del
ENST00000515133.5:n.43del
ENST00000621085.4:c.2del ENSP00000483421.1:p.Met1ArgfsTer4
ENST00000621628.4:c.2del ENSP00000480485.1:p.Met1ArgfsTer4
NM_000477.5:c.2del NP_000468.1:p.Met1ArgfsTer4
NM_000477.6:c.2del NP_000468.1:p.Met1ArgfsTer4
NM_000477.7:c.2del MANE Select NP_000468.1:p.Met1ArgfsTer4