Canonical Allele Identifier: CA127896

Gene: ALB

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413609G>A , CM000666.2:g.73413609G>A	GRCh38
NC_000004.11:g.74279326G>A , CM000666.1:g.74279326G>A	GRCh37
NC_000004.10:g.74498190G>A	NCBI36
NG_009291.1:g.14355G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1033G>A MANE Select	ENSP00000295897.4:p.Glu345Lys
ENST00000295897.8:c.1033G>A	ENSP00000295897.4:p.Glu345Lys
ENST00000401494.7:c.688G>A	ENSP00000384695.3:p.Glu230Lys
ENST00000415165.6:c.457G>A	ENSP00000401820.2:p.Glu153Lys
ENST00000476441.6:c.*312G>A	ENSP00000423727.1:n.*312G>A
ENST00000484992.1:n.353G>A
ENST00000503124.5:c.583G>A	ENSP00000421027.1:p.Glu195Lys
ENST00000504043.1:n.36G>A
ENST00000505649.5:n.719G>A
ENST00000509063.5:c.1033G>A	ENSP00000422784.1:p.Glu345Lys
ENST00000511370.1:c.566G>A
ENST00000621085.4:c.491-1497G>A	ENSP00000483421.1:n.491-1497G>A
ENST00000621628.4:c.487-1493G>A	ENSP00000480485.1:n.487-1493G>A
NM_000477.5:c.1033G>A	NP_000468.1:p.Glu345Lys
NM_000477.6:c.1033G>A	NP_000468.1:p.Glu345Lys
NM_000477.7:c.1033G>A MANE Select	NP_000468.1:p.Glu345Lys