Canonical Allele Identifier: CA357247266

Gene: ALB

Linked Data

• gnomAD v4: 4-73420290-G-A
• MyVariant Identifiers: chr4:g.74286007G>A (hg19) ; chr4:g.73420290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420290G>A , CM000666.2:g.73420290G>A	GRCh38
NC_000004.11:g.74286007G>A , CM000666.1:g.74286007G>A	GRCh37
NC_000004.10:g.74504871G>A	NCBI36
NG_009291.1:g.21036G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1822G>A MANE Select	ENSP00000295897.4:p.Gly608Ser
ENST00000295897.8:c.1822G>A	ENSP00000295897.4:p.Gly608Ser
ENST00000401494.7:c.1477G>A	ENSP00000384695.3:p.Gly493Ser
ENST00000415165.6:c.1246G>A	ENSP00000401820.2:p.Gly416Ser
ENST00000476441.6:c.*1101G>A	ENSP00000423727.1:n.*1101G>A
ENST00000495173.1:n.130G>A
ENST00000503124.5:c.1372G>A	ENSP00000421027.1:p.Gly458Ser
ENST00000505649.5:n.1369G>A
ENST00000508932.5:n.212G>A
ENST00000509063.5:c.1785+651G>A	ENSP00000422784.1:n.1785+651G>A
ENST00000511370.1:c.1355G>A
ENST00000621085.4:c.1183G>A	ENSP00000483421.1:p.Gly395Ser
ENST00000621628.4:c.1183G>A	ENSP00000480485.1:p.Gly395Ser
NM_000477.5:c.1822G>A	NP_000468.1:p.Gly608Ser
NM_000477.6:c.1822G>A	NP_000468.1:p.Gly608Ser
NM_000477.7:c.1822G>A MANE Select	NP_000468.1:p.Gly608Ser