Canonical Allele Identifier: CA1468143455
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415070A= , CM000666.2:g.73415070A= GRCh38
NC_000004.11:g.74280787A= , CM000666.1:g.74280787A= GRCh37
NC_000004.10:g.74499651A= NCBI36
NG_009291.1:g.15816A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1094A= MANE Select ENSP00000295897.4:p.Tyr365=
ENST00000295897.8:c.1094A= ENSP00000295897.4:p.Tyr365=
ENST00000401494.7:c.749A= ENSP00000384695.3:p.Tyr250=
ENST00000415165.6:c.518A= ENSP00000401820.2:p.Tyr173=
ENST00000476441.6:c.*373A= ENSP00000423727.1:n.*373A=
ENST00000484992.1:n.414A=
ENST00000503124.5:c.644A= ENSP00000421027.1:p.Tyr215=
ENST00000504043.1:n.97A=
ENST00000505649.5:n.780A=
ENST00000509063.5:c.1094A= ENSP00000422784.1:p.Tyr365=
ENST00000511370.1:c.627A=
ENST00000621085.4:c.491-36A= ENSP00000483421.1:n.491-36A=
ENST00000621628.4:c.487-32A= ENSP00000480485.1:n.487-32A=
NM_000477.5:c.1094A= NP_000468.1:p.Tyr365=
NM_000477.6:c.1094A= NP_000468.1:p.Tyr365=
NM_000477.7:c.1094A= MANE Select NP_000468.1:p.Tyr365=