Canonical Allele Identifier: CA357241091
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1076C>G MANE Select ENSP00000295897.4:p.Ala359Gly
ENST00000295897.8:c.1076C>G ENSP00000295897.4:p.Ala359Gly
ENST00000401494.7:c.731C>G ENSP00000384695.3:p.Ala244Gly
ENST00000415165.6:c.500C>G ENSP00000401820.2:p.Ala167Gly
ENST00000476441.6:c.*355C>G ENSP00000423727.1:n.*355C>G
ENST00000484992.1:n.396C>G
ENST00000503124.5:c.626C>G ENSP00000421027.1:p.Ala209Gly
ENST00000504043.1:n.79C>G
ENST00000505649.5:n.762C>G
ENST00000509063.5:c.1076C>G ENSP00000422784.1:p.Ala359Gly
ENST00000511370.1:c.609C>G
ENST00000621085.4:c.491-54C>G ENSP00000483421.1:n.491-54C>G
ENST00000621628.4:c.487-50C>G ENSP00000480485.1:n.487-50C>G
NM_000477.5:c.1076C>G NP_000468.1:p.Ala359Gly
NM_000477.6:c.1076C>G NP_000468.1:p.Ala359Gly
NM_000477.7:c.1076C>G MANE Select NP_000468.1:p.Ala359Gly