Canonical Allele Identifier: CA439800336

Gene: ALB

Linked Data

• gnomAD v4: 4-73415122-G-A
• MyVariant Identifiers: chr4:g.74280839G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415122G>A , CM000666.2:g.73415122G>A	GRCh38
NC_000004.11:g.74280839G>A , CM000666.1:g.74280839G>A	GRCh37
NC_000004.10:g.74499703G>A	NCBI36
NG_009291.1:g.15868G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1146G>A MANE Select	ENSP00000295897.4:p.Glu382=
ENST00000295897.8:c.1146G>A	ENSP00000295897.4:p.Glu382=
ENST00000401494.7:c.801G>A	ENSP00000384695.3:p.Glu267=
ENST00000415165.6:c.570G>A	ENSP00000401820.2:p.Glu190=
ENST00000476441.6:c.*425G>A	ENSP00000423727.1:n.*425G>A
ENST00000484992.1:n.466G>A
ENST00000503124.5:c.696G>A	ENSP00000421027.1:p.Glu232=
ENST00000504043.1:n.149G>A
ENST00000505649.5:n.832G>A
ENST00000509063.5:c.1146G>A	ENSP00000422784.1:p.Glu382=
ENST00000511370.1:c.679G>A
ENST00000621085.4:c.507G>A	ENSP00000483421.1:p.Glu169=
ENST00000621628.4:c.507G>A	ENSP00000480485.1:p.Glu169=
NM_000477.5:c.1146G>A	NP_000468.1:p.Glu382=
NM_000477.6:c.1146G>A	NP_000468.1:p.Glu382=
NM_000477.7:c.1146G>A MANE Select	NP_000468.1:p.Glu382=