Canonical Allele Identifier: CA798286233

Gene: ALB

Linked Data

• dbSNP Id: rs1250260879
• MyVariant Identifiers: chr4:g.74274318del (hg19) ; chr4:g.73408601del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408605del , CM000666.2:g.73408605del	GRCh38
NC_000004.11:g.74274322del , CM000666.1:g.74274322del	GRCh37
NC_000004.10:g.74493186del	NCBI36
NG_009291.1:g.9351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.282del MANE Select	ENSP00000295897.4:p.Phe94LeufsTer?
ENST00000295897.8:c.282del	ENSP00000295897.4:p.Phe94LeufsTer?
ENST00000401494.7:c.138-750del	ENSP00000384695.3:n.138-750del
ENST00000415165.6:c.138-3391del	ENSP00000401820.2:n.138-3391del
ENST00000441319.5:c.288del	ENSP00000392541.1:p.Phe96LeufsTer?
ENST00000476441.6:c.80-750del	ENSP00000423727.1:n.80-750del
ENST00000503124.5:c.33-750del	ENSP00000421027.1:n.33-750del
ENST00000509063.5:c.282del	ENSP00000422784.1:p.Phe94LeufsTer?
ENST00000510166.5:n.318del
ENST00000514786.1:n.251del
ENST00000515133.5:n.323del
ENST00000621085.4:c.282del	ENSP00000483421.1:p.Phe94LeufsTer?
ENST00000621628.4:c.282del	ENSP00000480485.1:p.Phe94LeufsTer?
NM_000477.5:c.282del	NP_000468.1:p.Phe94LeufsTer?
NM_000477.6:c.282del	NP_000468.1:p.Phe94LeufsTer?
NM_000477.7:c.282del MANE Select	NP_000468.1:p.Phe94LeufsTer?