Canonical Allele Identifier: CA357246576

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285328A>T (hg19) ; chr4:g.73419611A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419611A>T , CM000666.2:g.73419611A>T	GRCh38
NC_000004.11:g.74285328A>T , CM000666.1:g.74285328A>T	GRCh37
NC_000004.10:g.74504192A>T	NCBI36
NG_009291.1:g.20357A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1757A>T MANE Select	ENSP00000295897.4:p.Asp586Val
ENST00000295897.8:c.1757A>T	ENSP00000295897.4:p.Asp586Val
ENST00000401494.7:c.1412A>T	ENSP00000384695.3:p.Asp471Val
ENST00000415165.6:c.1181A>T	ENSP00000401820.2:p.Asp394Val
ENST00000476441.6:c.*1036A>T	ENSP00000423727.1:n.*1036A>T
ENST00000495173.1:n.65A>T
ENST00000503124.5:c.1307A>T	ENSP00000421027.1:p.Asp436Val
ENST00000505649.5:n.1304A>T
ENST00000508932.5:n.175+156A>T
ENST00000509063.5:c.1757A>T	ENSP00000422784.1:p.Asp586Val
ENST00000511370.1:c.1290A>T
ENST00000621085.4:c.1118A>T	ENSP00000483421.1:p.Asp373Val
ENST00000621628.4:c.1118A>T	ENSP00000480485.1:p.Asp373Val
NM_000477.5:c.1757A>T	NP_000468.1:p.Asp586Val
NM_000477.6:c.1757A>T	NP_000468.1:p.Asp586Val
NM_000477.7:c.1757A>T MANE Select	NP_000468.1:p.Asp586Val