Canonical Allele Identifier: CA170815
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 156312
ClinVar RCV Id: RCV000144396
dbSNP Id: rs77081291
MyVariant Identifiers: chr4:g.74283986del (hg19) chr4:g.73418269del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418269del , CM000666.2:g.73418269del GRCh38
NC_000004.11:g.74283986del , CM000666.1:g.74283986del GRCh37
NC_000004.10:g.74502850del NCBI36
NG_009291.1:g.19015del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1610del MANE Select ENSP00000295897.4:p.Ile537AsnfsTer21
ENST00000295897.8:c.1610del ENSP00000295897.4:p.Ile537AsnfsTer21
ENST00000401494.7:c.1265del ENSP00000384695.3:p.Ile422AsnfsTer21
ENST00000415165.6:c.1034del ENSP00000401820.2:p.Ile345AsnfsTer21
ENST00000476441.6:c.*889del ENSP00000423727.1:n.*889del
ENST00000486939.1:n.264del
ENST00000503124.5:c.1160del ENSP00000421027.1:p.Ile387AsnfsTer21
ENST00000505649.5:n.1157del
ENST00000509063.5:c.1610del ENSP00000422784.1:p.Ile537AsnfsTer21
ENST00000511370.1:c.1143del
ENST00000621085.4:c.971del ENSP00000483421.1:p.Ile324AsnfsTer21
ENST00000621628.4:c.971del ENSP00000480485.1:p.Ile324AsnfsTer21
NM_000477.5:c.1610del NP_000468.1:p.Ile537AsnfsTer21
NM_000477.6:c.1610del NP_000468.1:p.Ile537AsnfsTer21
NM_000477.7:c.1610del MANE Select NP_000468.1:p.Ile537AsnfsTer21
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