Canonical Allele Identifier: CA1064138221

Gene: ALB

Linked Data

• dbSNP Id: rs1718740543
• gnomAD v3: 4-73406785-ATTCT-A
• gnomAD v4: 4-73406785-ATTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406791_73406794del , CM000666.2:g.73406791_73406794del	GRCh38
NC_000004.11:g.74272508_74272511del , CM000666.1:g.74272508_74272511del	GRCh37
NC_000004.10:g.74491372_74491375del	NCBI36
NG_009291.1:g.7537_7540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+30_270+33del MANE Select	ENSP00000295897.4:n.270+30_270+33del
ENST00000295897.8:c.270+30_270+33del	ENSP00000295897.4:n.270+30_270+33del
ENST00000401494.7:c.137+1618_137+1621del	ENSP00000384695.3:n.137+1618_137+1621del
ENST00000415165.6:c.137+1618_137+1621del	ENSP00000401820.2:n.137+1618_137+1621del
ENST00000441319.5:c.276+30_276+33del	ENSP00000392541.1:n.276+30_276+33del
ENST00000476441.6:c.79+2385_79+2388del	ENSP00000423727.1:n.79+2385_79+2388del
ENST00000503124.5:c.32+30_32+33del	ENSP00000421027.1:n.32+30_32+33del
ENST00000509063.5:c.270+30_270+33del	ENSP00000422784.1:n.270+30_270+33del
ENST00000510166.5:n.306+30_306+33del
ENST00000514786.1:n.239+30_239+33del
ENST00000515133.5:n.311+30_311+33del
ENST00000621085.4:c.270+30_270+33del	ENSP00000483421.1:n.270+30_270+33del
ENST00000621628.4:c.270+30_270+33del	ENSP00000480485.1:n.270+30_270+33del
NM_000477.5:c.270+30_270+33del	NP_000468.1:n.270+30_270+33del
NM_000477.6:c.270+30_270+33del	NP_000468.1:n.270+30_270+33del
NM_000477.7:c.270+30_270+33del MANE Select	NP_000468.1:n.270+30_270+33del