Canonical Allele Identifier: CA170825

Gene: ALB

Linked Data

• ClinVar Variation Id: 156318
• ClinVar RCV Id: RCV000144402
• dbSNP Id: rs75000326
• MyVariant Identifiers: chr4:g.74285979dupA (hg19) ; chr4:g.73420262dupA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420262dup , CM000666.2:g.73420262dup	GRCh38
NC_000004.11:g.74285979dup , CM000666.1:g.74285979dup	GRCh37
NC_000004.10:g.74504843dup	NCBI36
NG_009291.1:g.21008dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1794dup MANE Select	ENSP00000295897.4:p.Leu599ThrfsTer30
ENST00000295897.8:c.1794dup	ENSP00000295897.4:p.Leu599ThrfsTer30
ENST00000401494.7:c.1449dup	ENSP00000384695.3:p.Leu484ThrfsTer30
ENST00000415165.6:c.1218dup	ENSP00000401820.2:p.Leu407ThrfsTer30
ENST00000476441.6:c.*1073dup	ENSP00000423727.1:n.*1073dup
ENST00000495173.1:n.102dup
ENST00000503124.5:c.1344dup	ENSP00000421027.1:p.Leu449ThrfsTer30
ENST00000505649.5:n.1341dup
ENST00000508932.5:n.184dup
ENST00000509063.5:c.1785+623dup	ENSP00000422784.1:n.1785+623dup
ENST00000511370.1:c.1327dup
ENST00000621085.4:c.1155dup	ENSP00000483421.1:p.Leu386ThrfsTer30
ENST00000621628.4:c.1155dup	ENSP00000480485.1:p.Leu386ThrfsTer30
NM_000477.5:c.1794dup	NP_000468.1:p.Leu599ThrfsTer30
NM_000477.6:c.1794dup	NP_000468.1:p.Leu599ThrfsTer30
NM_000477.7:c.1794dup MANE Select	NP_000468.1:p.Leu599ThrfsTer30