Canonical Allele Identifier: CA1468150868
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406656T= , CM000666.2:g.73406656T= GRCh38
NC_000004.11:g.74272373T= , CM000666.1:g.74272373T= GRCh37
NC_000004.10:g.74491237T= NCBI36
NG_009291.1:g.7402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.165T= MANE Select ENSP00000295897.4:p.Leu55=
ENST00000295897.8:c.165T= ENSP00000295897.4:p.Leu55=
ENST00000401494.7:c.137+1483T= ENSP00000384695.3:n.137+1483T=
ENST00000415165.6:c.137+1483T= ENSP00000401820.2:n.137+1483T=
ENST00000441319.5:c.171T= ENSP00000392541.1:p.Leu57=
ENST00000476441.6:c.79+2250T= ENSP00000423727.1:n.79+2250T=
ENST00000503124.5:c.-74T= ENSP00000421027.1:n.-74T=
ENST00000509063.5:c.165T= ENSP00000422784.1:p.Leu55=
ENST00000510166.5:n.201T=
ENST00000514786.1:n.134T=
ENST00000515133.5:n.206T=
ENST00000621085.4:c.165T= ENSP00000483421.1:p.Leu55=
ENST00000621628.4:c.165T= ENSP00000480485.1:p.Leu55=
NM_000477.5:c.165T= NP_000468.1:p.Leu55=
NM_000477.6:c.165T= NP_000468.1:p.Leu55=
NM_000477.7:c.165T= MANE Select NP_000468.1:p.Leu55=