Canonical Allele Identifier: CA127968

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415045G>A , CM000666.2:g.73415045G>A	GRCh38
NC_000004.11:g.74280762G>A , CM000666.1:g.74280762G>A	GRCh37
NC_000004.10:g.74499626G>A	NCBI36
NG_009291.1:g.15791G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1069G>A MANE Select	NP_000468.1:p.Glu357Lys
ENST00000295897.9:c.1069G>A MANE Select	ENSP00000295897.4:p.Glu357Lys
NM_000477.5:c.1069G>A	NP_000468.1:p.Glu357Lys
NM_000477.6:c.1069G>A	NP_000468.1:p.Glu357Lys
ENST00000295897.8:c.1069G>A	ENSP00000295897.4:p.Glu357Lys
ENST00000401494.7:c.724G>A	ENSP00000384695.3:p.Glu242Lys
ENST00000415165.6:c.493G>A	ENSP00000401820.2:p.Glu165Lys
ENST00000476441.6:c.*348G>A	ENSP00000423727.1:n.*348G>A
ENST00000484992.1:n.389G>A
ENST00000503124.5:c.619G>A	ENSP00000421027.1:p.Glu207Lys
ENST00000504043.1:n.72G>A
ENST00000505649.5:n.755G>A
ENST00000509063.5:c.1069G>A	ENSP00000422784.1:p.Glu357Lys
ENST00000511370.1:c.602G>A
ENST00000621085.4:c.491-61G>A	ENSP00000483421.1:n.491-61G>A
ENST00000621628.4:c.487-57G>A	ENSP00000480485.1:n.487-57G>A