Canonical Allele Identifier: CA357240520

Gene: ALB

Linked Data

• gnomAD v4: 4-73413454-A-T
• MyVariant Identifiers: chr4:g.74279171A>T (hg19) ; chr4:g.73413454A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413454A>T , CM000666.2:g.73413454A>T	GRCh38
NC_000004.11:g.74279171A>T , CM000666.1:g.74279171A>T	GRCh37
NC_000004.10:g.74498035A>T	NCBI36
NG_009291.1:g.14200A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.878A>T MANE Select	ENSP00000295897.4:p.Asp293Val
ENST00000295897.8:c.878A>T	ENSP00000295897.4:p.Asp293Val
ENST00000401494.7:c.533A>T	ENSP00000384695.3:p.Asp178Val
ENST00000415165.6:c.302A>T	ENSP00000401820.2:p.Asp101Val
ENST00000476441.6:c.*157A>T	ENSP00000423727.1:n.*157A>T
ENST00000484992.1:n.198A>T
ENST00000503124.5:c.428A>T	ENSP00000421027.1:p.Asp143Val
ENST00000505649.5:n.564A>T
ENST00000509063.5:c.878A>T	ENSP00000422784.1:p.Asp293Val
ENST00000511370.1:c.411A>T
ENST00000621085.4:c.491-1652A>T	ENSP00000483421.1:n.491-1652A>T
ENST00000621628.4:c.487-1648A>T	ENSP00000480485.1:n.487-1648A>T
NM_000477.5:c.878A>T	NP_000468.1:p.Asp293Val
NM_000477.6:c.878A>T	NP_000468.1:p.Asp293Val
NM_000477.7:c.878A>T MANE Select	NP_000468.1:p.Asp293Val