Canonical Allele Identifier: CA357238340
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409467G>C , CM000666.2:g.73409467G>C GRCh38
NC_000004.11:g.74275184G>C , CM000666.1:g.74275184G>C GRCh37
NC_000004.10:g.74494048G>C NCBI36
NG_009291.1:g.10213G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.595G>C MANE Select ENSP00000295897.4:p.Ala199Pro
ENST00000295897.8:c.595G>C ENSP00000295897.4:p.Ala199Pro
ENST00000401494.7:c.250G>C ENSP00000384695.3:p.Ala84Pro
ENST00000415165.6:c.138-2529G>C ENSP00000401820.2:n.138-2529G>C
ENST00000476441.6:c.192G>C ENSP00000423727.1:p.Lys64Asn
ENST00000503124.5:c.145G>C ENSP00000421027.1:p.Ala49Pro
ENST00000505649.5:n.281G>C
ENST00000509063.5:c.595G>C ENSP00000422784.1:p.Ala199Pro
ENST00000511370.1:c.128G>C
ENST00000514786.1:n.564G>C
ENST00000621085.4:c.490+105G>C ENSP00000483421.1:n.490+105G>C
ENST00000621628.4:c.486+391G>C ENSP00000480485.1:n.486+391G>C
NM_000477.5:c.595G>C NP_000468.1:p.Ala199Pro
NM_000477.6:c.595G>C NP_000468.1:p.Ala199Pro
NM_000477.7:c.595G>C MANE Select NP_000468.1:p.Ala199Pro