Canonical Allele Identifier: CA645517844

Gene: ALB

Linked Data

• COSMIC: COSM1727588

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409407_73409418del , CM000666.2:g.73409407_73409418del	GRCh38
NC_000004.11:g.74275124_74275135del , CM000666.1:g.74275124_74275135del	GRCh37
NC_000004.10:g.74493988_74493999del	NCBI36
NG_009291.1:g.10153_10164del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.535_546del MANE Select	ENSP00000295897.4:p.Leu179_Ala182del
ENST00000295897.8:c.535_546del	ENSP00000295897.4:p.Leu179_Ala182del
ENST00000401494.7:c.190_201del	ENSP00000384695.3:p.Leu64_Ala67del
ENST00000415165.6:c.138-2589_138-2578del	ENSP00000401820.2:n.138-2589_138-2578del
ENST00000441319.5:c.541_552del	ENSP00000392541.1:p.Leu181_Ala184del
ENST00000476441.6:c.132_143del	ENSP00000423727.1:p.Phe45_Leu48del
ENST00000503124.5:c.85_96del	ENSP00000421027.1:p.Leu29_Ala32del
ENST00000505649.5:n.221_232del
ENST00000509063.5:c.535_546del	ENSP00000422784.1:p.Leu179_Ala182del
ENST00000511370.1:c.68_79del
ENST00000514786.1:n.504_515del
ENST00000621085.4:c.490+45_490+56del	ENSP00000483421.1:n.490+45_490+56del
ENST00000621628.4:c.486+331_486+342del	ENSP00000480485.1:n.486+331_486+342del
NM_000477.5:c.535_546del	NP_000468.1:p.Leu179_Ala182del
NM_000477.6:c.535_546del	NP_000468.1:p.Leu179_Ala182del
NM_000477.7:c.535_546del MANE Select	NP_000468.1:p.Leu179_Ala182del