Canonical Allele Identifier: CA648962651

Gene: ALB

Linked Data

• COSMIC: COSN1300815

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406585_73406588del , CM000666.2:g.73406585_73406588del	GRCh38
NC_000004.11:g.74272302_74272305del , CM000666.1:g.74272302_74272305del	GRCh37
NC_000004.10:g.74491166_74491169del	NCBI36
NG_009291.1:g.7331_7334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-44_138-41del MANE Select	ENSP00000295897.4:n.138-44_138-41del
ENST00000295897.8:c.138-44_138-41del	ENSP00000295897.4:n.138-44_138-41del
ENST00000401494.7:c.137+1412_137+1415del	ENSP00000384695.3:n.137+1412_137+1415del
ENST00000415165.6:c.137+1412_137+1415del	ENSP00000401820.2:n.137+1412_137+1415del
ENST00000441319.5:c.144-44_144-41del	ENSP00000392541.1:n.144-44_144-41del
ENST00000476441.6:c.79+2179_79+2182del	ENSP00000423727.1:n.79+2179_79+2182del
ENST00000503124.5:c.-101-44_-101-41del	ENSP00000421027.1:n.-101-44_-101-41del
ENST00000509063.5:c.138-44_138-41del	ENSP00000422784.1:n.138-44_138-41del
ENST00000510166.5:n.174-44_174-41del
ENST00000514786.1:n.107-44_107-41del
ENST00000515133.5:n.179-44_179-41del
ENST00000621085.4:c.138-44_138-41del	ENSP00000483421.1:n.138-44_138-41del
ENST00000621628.4:c.138-44_138-41del	ENSP00000480485.1:n.138-44_138-41del
NM_000477.5:c.138-44_138-41del	NP_000468.1:n.138-44_138-41del
NM_000477.6:c.138-44_138-41del	NP_000468.1:n.138-44_138-41del
NM_000477.7:c.138-44_138-41del MANE Select	NP_000468.1:n.138-44_138-41del