Canonical Allele Identifier: CA357244742

Gene: ALB

Linked Data

• gnomAD v4: 4-73418214-G-A
• MyVariant Identifiers: chr4:g.74283931G>A (hg19) ; chr4:g.73418214G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418214G>A , CM000666.2:g.73418214G>A	GRCh38
NC_000004.11:g.74283931G>A , CM000666.1:g.74283931G>A	GRCh37
NC_000004.10:g.74502795G>A	NCBI36
NG_009291.1:g.18960G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1555G>A MANE Select	ENSP00000295897.4:p.Glu519Lys
ENST00000295897.8:c.1555G>A	ENSP00000295897.4:p.Glu519Lys
ENST00000401494.7:c.1210G>A	ENSP00000384695.3:p.Glu404Lys
ENST00000415165.6:c.979G>A	ENSP00000401820.2:p.Glu327Lys
ENST00000476441.6:c.*834G>A	ENSP00000423727.1:n.*834G>A
ENST00000486939.1:n.209G>A
ENST00000503124.5:c.1105G>A	ENSP00000421027.1:p.Glu369Lys
ENST00000505649.5:n.1102G>A
ENST00000509063.5:c.1555G>A	ENSP00000422784.1:p.Glu519Lys
ENST00000511370.1:c.1088G>A
ENST00000621085.4:c.916G>A	ENSP00000483421.1:p.Glu306Lys
ENST00000621628.4:c.916G>A	ENSP00000480485.1:p.Glu306Lys
NM_000477.5:c.1555G>A	NP_000468.1:p.Glu519Lys
NM_000477.6:c.1555G>A	NP_000468.1:p.Glu519Lys
NM_000477.7:c.1555G>A MANE Select	NP_000468.1:p.Glu519Lys