Canonical Allele Identifier: CA439800392

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280881A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415164A>G , CM000666.2:g.73415164A>G	GRCh38
NC_000004.11:g.74280881A>G , CM000666.1:g.74280881A>G	GRCh37
NC_000004.10:g.74499745A>G	NCBI36
NG_009291.1:g.15910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1188A>G MANE Select	ENSP00000295897.4:p.Lys396=
ENST00000295897.8:c.1188A>G	ENSP00000295897.4:p.Lys396=
ENST00000401494.7:c.843A>G	ENSP00000384695.3:p.Lys281=
ENST00000415165.6:c.612A>G	ENSP00000401820.2:p.Lys204=
ENST00000476441.6:c.*467A>G	ENSP00000423727.1:n.*467A>G
ENST00000484992.1:n.508A>G
ENST00000503124.5:c.738A>G	ENSP00000421027.1:p.Lys246=
ENST00000504043.1:n.191A>G
ENST00000505649.5:n.874A>G
ENST00000509063.5:c.1188A>G	ENSP00000422784.1:p.Lys396=
ENST00000511370.1:c.721A>G
ENST00000621085.4:c.549A>G	ENSP00000483421.1:p.Lys183=
ENST00000621628.4:c.549A>G	ENSP00000480485.1:p.Lys183=
NM_000477.5:c.1188A>G	NP_000468.1:p.Lys396=
NM_000477.6:c.1188A>G	NP_000468.1:p.Lys396=
NM_000477.7:c.1188A>G MANE Select	NP_000468.1:p.Lys396=