Canonical Allele Identifier: CA439801116

Gene: ALB

Linked Data

• gnomAD v4: 4-73420295-A-G
• MyVariant Identifiers: chr4:g.74286012A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420295A>G , CM000666.2:g.73420295A>G	GRCh38
NC_000004.11:g.74286012A>G , CM000666.1:g.74286012A>G	GRCh37
NC_000004.10:g.74504876A>G	NCBI36
NG_009291.1:g.21041A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1827A>G MANE Select	ENSP00000295897.4:p.Leu609=
ENST00000295897.8:c.1827A>G	ENSP00000295897.4:p.Leu609=
ENST00000401494.7:c.1482A>G	ENSP00000384695.3:p.Leu494=
ENST00000415165.6:c.1251A>G	ENSP00000401820.2:p.Leu417=
ENST00000476441.6:c.*1106A>G	ENSP00000423727.1:n.*1106A>G
ENST00000495173.1:n.135A>G
ENST00000503124.5:c.1377A>G	ENSP00000421027.1:p.Leu459=
ENST00000505649.5:n.1374A>G
ENST00000508932.5:n.217A>G
ENST00000509063.5:c.1785+656A>G	ENSP00000422784.1:n.1785+656A>G
ENST00000511370.1:c.1360A>G
ENST00000621085.4:c.1188A>G	ENSP00000483421.1:p.Leu396=
ENST00000621628.4:c.1188A>G	ENSP00000480485.1:p.Leu396=
NM_000477.5:c.1827A>G	NP_000468.1:p.Leu609=
NM_000477.6:c.1827A>G	NP_000468.1:p.Leu609=
NM_000477.7:c.1827A>G MANE Select	NP_000468.1:p.Leu609=