Canonical Allele Identifier: CA2578063689
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404338del , CM000666.2:g.73404338del GRCh38
NC_000004.11:g.74270055del , CM000666.1:g.74270055del GRCh37
NC_000004.10:g.74488919del NCBI36
NG_009291.1:g.5084del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.11del MANE Select ENSP00000295897.4:p.Val4GlufsTer?
ENST00000295897.8:c.11del ENSP00000295897.4:p.Val4GlufsTer?
ENST00000401494.7:c.11del ENSP00000384695.3:p.Val4GlufsTer?
ENST00000415165.6:c.11del ENSP00000401820.2:p.Val4GlufsTer?
ENST00000441319.5:c.48-31del ENSP00000392541.1:n.48-31del
ENST00000476441.6:c.11del ENSP00000423727.1:p.Val4GlufsTer27
ENST00000503124.5:c.-170del ENSP00000421027.1:n.-170del
ENST00000509063.5:c.11del ENSP00000422784.1:p.Val4GlufsTer?
ENST00000510166.5:n.52del
ENST00000514786.1:n.48+2del
ENST00000515133.5:n.52del
ENST00000621085.4:c.11del ENSP00000483421.1:p.Val4GlufsTer?
ENST00000621628.4:c.11del ENSP00000480485.1:p.Val4GlufsTer?
NM_000477.5:c.11del NP_000468.1:p.Val4GlufsTer?
NM_000477.6:c.11del NP_000468.1:p.Val4GlufsTer?
NM_000477.7:c.11del MANE Select NP_000468.1:p.Val4GlufsTer?