Canonical Allele Identifier: CA439801109

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286006A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420289A>G , CM000666.2:g.73420289A>G	GRCh38
NC_000004.11:g.74286006A>G , CM000666.1:g.74286006A>G	GRCh37
NC_000004.10:g.74504870A>G	NCBI36
NG_009291.1:g.21035A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1821A>G MANE Select	ENSP00000295897.4:p.Leu607=
ENST00000295897.8:c.1821A>G	ENSP00000295897.4:p.Leu607=
ENST00000401494.7:c.1476A>G	ENSP00000384695.3:p.Leu492=
ENST00000415165.6:c.1245A>G	ENSP00000401820.2:p.Leu415=
ENST00000476441.6:c.*1100A>G	ENSP00000423727.1:n.*1100A>G
ENST00000495173.1:n.129A>G
ENST00000503124.5:c.1371A>G	ENSP00000421027.1:p.Leu457=
ENST00000505649.5:n.1368A>G
ENST00000508932.5:n.211A>G
ENST00000509063.5:c.1785+650A>G	ENSP00000422784.1:n.1785+650A>G
ENST00000511370.1:c.1354A>G
ENST00000621085.4:c.1182A>G	ENSP00000483421.1:p.Leu394=
ENST00000621628.4:c.1182A>G	ENSP00000480485.1:p.Leu394=
NM_000477.5:c.1821A>G	NP_000468.1:p.Leu607=
NM_000477.6:c.1821A>G	NP_000468.1:p.Leu607=
NM_000477.7:c.1821A>G MANE Select	NP_000468.1:p.Leu607=