Canonical Allele Identifier: CA1468146957

Gene: ALB

Linked Data

• dbSNP Id: rs1719067676

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418266del , CM000666.2:g.73418266del	GRCh38
NC_000004.11:g.74283983del , CM000666.1:g.74283983del	GRCh37
NC_000004.10:g.74502847del	NCBI36
NG_009291.1:g.19012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1607del MANE Select	ENSP00000295897.4:p.Asp536ValfsTer22
ENST00000295897.8:c.1607del	ENSP00000295897.4:p.Asp536ValfsTer22
ENST00000401494.7:c.1262del	ENSP00000384695.3:p.Asp421ValfsTer22
ENST00000415165.6:c.1031del	ENSP00000401820.2:p.Asp344ValfsTer22
ENST00000476441.6:c.*886del	ENSP00000423727.1:n.*886del
ENST00000486939.1:n.261del
ENST00000503124.5:c.1157del	ENSP00000421027.1:p.Asp386ValfsTer22
ENST00000505649.5:n.1154del
ENST00000509063.5:c.1607del	ENSP00000422784.1:p.Asp536ValfsTer22
ENST00000511370.1:c.1140del
ENST00000621085.4:c.968del	ENSP00000483421.1:p.Asp323ValfsTer22
ENST00000621628.4:c.968del	ENSP00000480485.1:p.Asp323ValfsTer22
NM_000477.5:c.1607del	NP_000468.1:p.Asp536ValfsTer22
NM_000477.6:c.1607del	NP_000468.1:p.Asp536ValfsTer22
NM_000477.7:c.1607del MANE Select	NP_000468.1:p.Asp536ValfsTer22