Canonical Allele Identifier: CA439801076

Gene: ALB

Linked Data

• gnomAD v3: 4-73420262-A-G
• gnomAD v4: 4-73420262-A-G
• MyVariant Identifiers: chr4:g.74285979A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420262A>G , CM000666.2:g.73420262A>G	GRCh38
NC_000004.11:g.74285979A>G , CM000666.1:g.74285979A>G	GRCh37
NC_000004.10:g.74504843A>G	NCBI36
NG_009291.1:g.21008A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1794A>G MANE Select	ENSP00000295897.4:p.Lys598=
ENST00000295897.8:c.1794A>G	ENSP00000295897.4:p.Lys598=
ENST00000401494.7:c.1449A>G	ENSP00000384695.3:p.Lys483=
ENST00000415165.6:c.1218A>G	ENSP00000401820.2:p.Lys406=
ENST00000476441.6:c.*1073A>G	ENSP00000423727.1:n.*1073A>G
ENST00000495173.1:n.102A>G
ENST00000503124.5:c.1344A>G	ENSP00000421027.1:p.Lys448=
ENST00000505649.5:n.1341A>G
ENST00000508932.5:n.184A>G
ENST00000509063.5:c.1785+623A>G	ENSP00000422784.1:n.1785+623A>G
ENST00000511370.1:c.1327A>G
ENST00000621085.4:c.1155A>G	ENSP00000483421.1:p.Lys385=
ENST00000621628.4:c.1155A>G	ENSP00000480485.1:p.Lys385=
NM_000477.5:c.1794A>G	NP_000468.1:p.Lys598=
NM_000477.6:c.1794A>G	NP_000468.1:p.Lys598=
NM_000477.7:c.1794A>G MANE Select	NP_000468.1:p.Lys598=