Canonical Allele Identifier: CA2740542118

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408795_73408800del , CM000666.2:g.73408795_73408800del	GRCh38
NC_000004.11:g.74274512_74274517del , CM000666.1:g.74274512_74274517del	GRCh37
NC_000004.10:g.74493376_74493381del	NCBI36
NG_009291.1:g.9541_9546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.472_477del MANE Select	ENSP00000295897.4:p.Phe158_Leu159del
ENST00000295897.8:c.472_477del	ENSP00000295897.4:p.Phe158_Leu159del
ENST00000401494.7:c.138-560_138-555del	ENSP00000384695.3:n.138-560_138-555del
ENST00000415165.6:c.138-3201_138-3196del	ENSP00000401820.2:n.138-3201_138-3196del
ENST00000441319.5:c.478_483del	ENSP00000392541.1:p.Phe160_Leu161del
ENST00000476441.6:c.80-560_80-555del	ENSP00000423727.1:n.80-560_80-555del
ENST00000503124.5:c.33-560_33-555del	ENSP00000421027.1:n.33-560_33-555del
ENST00000505649.5:n.158_163del
ENST00000509063.5:c.472_477del	ENSP00000422784.1:p.Phe158_Leu159del
ENST00000510166.5:n.508_513del
ENST00000514786.1:n.441_446del
ENST00000515133.5:n.513_518del
ENST00000621085.4:c.472_477del	ENSP00000483421.1:p.Phe158_Leu159del
ENST00000621628.4:c.472_477del	ENSP00000480485.1:p.Phe158_Leu159del
NM_000477.5:c.472_477del	NP_000468.1:p.Phe158_Leu159del
NM_000477.6:c.472_477del	NP_000468.1:p.Phe158_Leu159del
NM_000477.7:c.472_477del MANE Select	NP_000468.1:p.Phe158_Leu159del