Canonical Allele Identifier: CA439801002

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285338G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419621G>A , CM000666.2:g.73419621G>A	GRCh38
NC_000004.11:g.74285338G>A , CM000666.1:g.74285338G>A	GRCh37
NC_000004.10:g.74504202G>A	NCBI36
NG_009291.1:g.20367G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1767G>A MANE Select	ENSP00000295897.4:p.Glu589=
ENST00000295897.8:c.1767G>A	ENSP00000295897.4:p.Glu589=
ENST00000401494.7:c.1422G>A	ENSP00000384695.3:p.Glu474=
ENST00000415165.6:c.1191G>A	ENSP00000401820.2:p.Glu397=
ENST00000476441.6:c.*1046G>A	ENSP00000423727.1:n.*1046G>A
ENST00000495173.1:n.75G>A
ENST00000503124.5:c.1317G>A	ENSP00000421027.1:p.Glu439=
ENST00000505649.5:n.1314G>A
ENST00000508932.5:n.175+166G>A
ENST00000509063.5:c.1767G>A	ENSP00000422784.1:p.Glu589=
ENST00000511370.1:c.1300G>A
ENST00000621085.4:c.1128G>A	ENSP00000483421.1:p.Glu376=
ENST00000621628.4:c.1128G>A	ENSP00000480485.1:p.Glu376=
NM_000477.5:c.1767G>A	NP_000468.1:p.Glu589=
NM_000477.6:c.1767G>A	NP_000468.1:p.Glu589=
NM_000477.7:c.1767G>A MANE Select	NP_000468.1:p.Glu589=