Canonical Allele Identifier: CA127910

Gene: ALB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73416280G>A , CM000666.2:g.73416280G>A	GRCh38
NC_000004.11:g.74281997G>A , CM000666.1:g.74281997G>A	GRCh37
NC_000004.10:g.74500861G>A	NCBI36
NG_009291.1:g.17026G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1216G>A MANE Select	ENSP00000295897.4:p.Glu406Lys
ENST00000295897.8:c.1216G>A	ENSP00000295897.4:p.Glu406Lys
ENST00000401494.7:c.871G>A	ENSP00000384695.3:p.Glu291Lys
ENST00000415165.6:c.640G>A	ENSP00000401820.2:p.Glu214Lys
ENST00000476441.6:c.*495G>A	ENSP00000423727.1:n.*495G>A
ENST00000484992.1:n.536G>A
ENST00000503124.5:c.766G>A	ENSP00000421027.1:p.Glu256Lys
ENST00000505649.5:n.902G>A
ENST00000509063.5:c.1216G>A	ENSP00000422784.1:p.Glu406Lys
ENST00000511370.1:c.749G>A
ENST00000621085.4:c.577G>A	ENSP00000483421.1:p.Glu193Lys
ENST00000621628.4:c.577G>A	ENSP00000480485.1:p.Glu193Lys
NM_000477.5:c.1216G>A	NP_000468.1:p.Glu406Lys
NM_000477.6:c.1216G>A	NP_000468.1:p.Glu406Lys
NM_000477.7:c.1216G>A MANE Select	NP_000468.1:p.Glu406Lys