Canonical Allele Identifier: CA357241090
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415052C>A , CM000666.2:g.73415052C>A GRCh38
NC_000004.11:g.74280769C>A , CM000666.1:g.74280769C>A GRCh37
NC_000004.10:g.74499633C>A NCBI36
NG_009291.1:g.15798C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1076C>A MANE Select ENSP00000295897.4:p.Ala359Glu
ENST00000295897.8:c.1076C>A ENSP00000295897.4:p.Ala359Glu
ENST00000401494.7:c.731C>A ENSP00000384695.3:p.Ala244Glu
ENST00000415165.6:c.500C>A ENSP00000401820.2:p.Ala167Glu
ENST00000476441.6:c.*355C>A ENSP00000423727.1:n.*355C>A
ENST00000484992.1:n.396C>A
ENST00000503124.5:c.626C>A ENSP00000421027.1:p.Ala209Glu
ENST00000504043.1:n.79C>A
ENST00000505649.5:n.762C>A
ENST00000509063.5:c.1076C>A ENSP00000422784.1:p.Ala359Glu
ENST00000511370.1:c.609C>A
ENST00000621085.4:c.491-54C>A ENSP00000483421.1:n.491-54C>A
ENST00000621628.4:c.487-50C>A ENSP00000480485.1:n.487-50C>A
NM_000477.5:c.1076C>A NP_000468.1:p.Ala359Glu
NM_000477.6:c.1076C>A NP_000468.1:p.Ala359Glu
NM_000477.7:c.1076C>A MANE Select NP_000468.1:p.Ala359Glu