Canonical Allele Identifier: CA2670966769

Gene: ALB

Linked Data

• gnomAD v4: 4-73420283-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420284dup , CM000666.2:g.73420284dup	GRCh38
NC_000004.11:g.74286001dup , CM000666.1:g.74286001dup	GRCh37
NC_000004.10:g.74504865dup	NCBI36
NG_009291.1:g.21030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1816dup MANE Select	ENSP00000295897.4:p.Ala606GlyfsTer23
ENST00000295897.8:c.1816dup	ENSP00000295897.4:p.Ala606GlyfsTer23
ENST00000401494.7:c.1471dup	ENSP00000384695.3:p.Ala491GlyfsTer23
ENST00000415165.6:c.1240dup	ENSP00000401820.2:p.Ala414GlyfsTer23
ENST00000476441.6:c.*1095dup	ENSP00000423727.1:n.*1095dup
ENST00000495173.1:n.124dup
ENST00000503124.5:c.1366dup	ENSP00000421027.1:p.Ala456GlyfsTer23
ENST00000505649.5:n.1363dup
ENST00000508932.5:n.206dup
ENST00000509063.5:c.1785+645dup	ENSP00000422784.1:n.1785+645dup
ENST00000511370.1:c.1349dup
ENST00000621085.4:c.1177dup	ENSP00000483421.1:p.Ala393GlyfsTer23
ENST00000621628.4:c.1177dup	ENSP00000480485.1:p.Ala393GlyfsTer23
NM_000477.5:c.1816dup	NP_000468.1:p.Ala606GlyfsTer23
NM_000477.6:c.1816dup	NP_000468.1:p.Ala606GlyfsTer23
NM_000477.7:c.1816dup MANE Select	NP_000468.1:p.Ala606GlyfsTer23