Canonical Allele Identifier: CA1468148854

Gene: ALB

Linked Data

• dbSNP Id: rs1719111769

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420273dup , CM000666.2:g.73420273dup	GRCh38
NC_000004.11:g.74285990dup , CM000666.1:g.74285990dup	GRCh37
NC_000004.10:g.74504854dup	NCBI36
NG_009291.1:g.21019dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1805dup MANE Select	ENSP00000295897.4:p.Ser603LysfsTer26
ENST00000295897.8:c.1805dup	ENSP00000295897.4:p.Ser603LysfsTer26
ENST00000401494.7:c.1460dup	ENSP00000384695.3:p.Ser488LysfsTer26
ENST00000415165.6:c.1229dup	ENSP00000401820.2:p.Ser411LysfsTer26
ENST00000476441.6:c.*1084dup	ENSP00000423727.1:n.*1084dup
ENST00000495173.1:n.113dup
ENST00000503124.5:c.1355dup	ENSP00000421027.1:p.Ser453LysfsTer26
ENST00000505649.5:n.1352dup
ENST00000508932.5:n.195dup
ENST00000509063.5:c.1785+634dup	ENSP00000422784.1:n.1785+634dup
ENST00000511370.1:c.1338dup
ENST00000621085.4:c.1166dup	ENSP00000483421.1:p.Ser390LysfsTer26
ENST00000621628.4:c.1166dup	ENSP00000480485.1:p.Ser390LysfsTer26
NM_000477.5:c.1805dup	NP_000468.1:p.Ser603LysfsTer26
NM_000477.6:c.1805dup	NP_000468.1:p.Ser603LysfsTer26
NM_000477.7:c.1805dup MANE Select	NP_000468.1:p.Ser603LysfsTer26