Canonical Allele Identifier: CA1468150617

Gene: ALB

Linked Data

• dbSNP Id: rs1718729378

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406402_73406403del , CM000666.2:g.73406402_73406403del	GRCh38
NC_000004.11:g.74272119_74272120del , CM000666.1:g.74272119_74272120del	GRCh37
NC_000004.10:g.74490983_74490984del	NCBI36
NG_009291.1:g.7148_7149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-227_138-226del MANE Select	ENSP00000295897.4:n.138-227_138-226del
ENST00000295897.8:c.138-227_138-226del	ENSP00000295897.4:n.138-227_138-226del
ENST00000401494.7:c.137+1229_137+1230del	ENSP00000384695.3:n.137+1229_137+1230del
ENST00000415165.6:c.137+1229_137+1230del	ENSP00000401820.2:n.137+1229_137+1230del
ENST00000441319.5:c.144-227_144-226del	ENSP00000392541.1:n.144-227_144-226del
ENST00000476441.6:c.79+1996_79+1997del	ENSP00000423727.1:n.79+1996_79+1997del
ENST00000503124.5:c.-101-227_-101-226del	ENSP00000421027.1:n.-101-227_-101-226del
ENST00000509063.5:c.138-227_138-226del	ENSP00000422784.1:n.138-227_138-226del
ENST00000510166.5:n.174-227_174-226del
ENST00000514786.1:n.107-227_107-226del
ENST00000515133.5:n.179-227_179-226del
ENST00000621085.4:c.138-227_138-226del	ENSP00000483421.1:n.138-227_138-226del
ENST00000621628.4:c.138-227_138-226del	ENSP00000480485.1:n.138-227_138-226del
NM_000477.5:c.138-227_138-226del	NP_000468.1:n.138-227_138-226del
NM_000477.6:c.138-227_138-226del	NP_000468.1:n.138-227_138-226del
NM_000477.7:c.138-227_138-226del MANE Select	NP_000468.1:n.138-227_138-226del