Canonical Allele Identifier: CA1468148446
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404321T= , CM000666.2:g.73404321T= GRCh38
NC_000004.11:g.74270038T= , CM000666.1:g.74270038T= GRCh37
NC_000004.10:g.74488902T= NCBI36
NG_009291.1:g.5067T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-7T= MANE Select ENSP00000295897.4:n.-7T=
ENST00000295897.8:c.-7T= ENSP00000295897.4:n.-7T=
ENST00000401494.7:c.-7T= ENSP00000384695.3:n.-7T=
ENST00000415165.6:c.-7T= ENSP00000401820.2:n.-7T=
ENST00000441319.5:n.48-48T= ENSP00000392541.1:n.48-48T=
ENST00000476441.6:c.-7T= ENSP00000423727.1:n.-7T=
ENST00000503124.5:c.-187T= ENSP00000421027.1:n.-187T=
ENST00000509063.5:c.-7T= ENSP00000422784.1:n.-7T=
ENST00000510166.5:n.35T=
ENST00000514786.1:n.33T=
ENST00000515133.5:n.35T=
ENST00000621085.4:c.-7T= ENSP00000483421.1:n.-7T=
ENST00000621628.4:c.-7T= ENSP00000480485.1:n.-7T=
NM_000477.5:c.-7T= NP_000468.1:n.-7T=
NM_000477.6:c.-7T= NP_000468.1:n.-7T=
NM_000477.7:c.-7T= MANE Select NP_000468.1:n.-7T=