Canonical Allele Identifier: CA2586973901

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406723_73406724del , CM000666.2:g.73406723_73406724del	GRCh38
NC_000004.11:g.74272440_74272441del , CM000666.1:g.74272440_74272441del	GRCh37
NC_000004.10:g.74491304_74491305del	NCBI36
NG_009291.1:g.7469_7470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.232_233del MANE Select	ENSP00000295897.4:p.Val78CysfsTer2
ENST00000295897.8:c.232_233del	ENSP00000295897.4:p.Val78CysfsTer2
ENST00000401494.7:c.137+1550_137+1551del	ENSP00000384695.3:n.137+1550_137+1551del
ENST00000415165.6:c.137+1550_137+1551del	ENSP00000401820.2:n.137+1550_137+1551del
ENST00000441319.5:c.238_239del	ENSP00000392541.1:p.Val80CysfsTer2
ENST00000476441.6:c.79+2317_79+2318del	ENSP00000423727.1:n.79+2317_79+2318del
ENST00000503124.5:c.-7_-6del	ENSP00000421027.1:n.-7_-6del
ENST00000509063.5:c.232_233del	ENSP00000422784.1:p.Val78CysfsTer2
ENST00000510166.5:n.268_269del
ENST00000514786.1:n.201_202del
ENST00000515133.5:n.273_274del
ENST00000621085.4:c.232_233del	ENSP00000483421.1:p.Val78CysfsTer2
ENST00000621628.4:c.232_233del	ENSP00000480485.1:p.Val78CysfsTer2
NM_000477.5:c.232_233del	NP_000468.1:p.Val78CysfsTer2
NM_000477.6:c.232_233del	NP_000468.1:p.Val78CysfsTer2
NM_000477.7:c.232_233del MANE Select	NP_000468.1:p.Val78CysfsTer2