Canonical Allele Identifier: CA357237254
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408756G>T , CM000666.2:g.73408756G>T GRCh38
NC_000004.11:g.74274473G>T , CM000666.1:g.74274473G>T GRCh37
NC_000004.10:g.74493337G>T NCBI36
NG_009291.1:g.9502G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.433G>T MANE Select ENSP00000295897.4:p.Asp145Tyr
ENST00000295897.8:c.433G>T ENSP00000295897.4:p.Asp145Tyr
ENST00000401494.7:c.138-599G>T ENSP00000384695.3:n.138-599G>T
ENST00000415165.6:c.138-3240G>T ENSP00000401820.2:n.138-3240G>T
ENST00000441319.5:c.439G>T ENSP00000392541.1:p.Asp147Tyr
ENST00000476441.6:c.80-599G>T ENSP00000423727.1:n.80-599G>T
ENST00000503124.5:c.33-599G>T ENSP00000421027.1:n.33-599G>T
ENST00000505649.5:n.119G>T
ENST00000509063.5:c.433G>T ENSP00000422784.1:p.Asp145Tyr
ENST00000510166.5:n.469G>T
ENST00000514786.1:n.402G>T
ENST00000515133.5:n.474G>T
ENST00000621085.4:c.433G>T ENSP00000483421.1:p.Asp145Tyr
ENST00000621628.4:c.433G>T ENSP00000480485.1:p.Asp145Tyr
NM_000477.5:c.433G>T NP_000468.1:p.Asp145Tyr
NM_000477.6:c.433G>T NP_000468.1:p.Asp145Tyr
NM_000477.7:c.433G>T MANE Select NP_000468.1:p.Asp145Tyr