Canonical Allele Identifier: CA2959488

Gene: ALB

Linked Data

• dbSNP Id: rs762322697
• ExAC: 4:74279192 AGGAATGCT / A
• gnomAD v2: 4-74279192-AGGAATGCT-A
• MyVariant Identifiers: chr4:g.74279193_74279200del (hg19) ; chr4:g.73413476_73413483del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413477_73413484del , CM000666.2:g.73413477_73413484del	GRCh38
NC_000004.11:g.74279194_74279201del , CM000666.1:g.74279194_74279201del	GRCh37
NC_000004.10:g.74498058_74498065del	NCBI36
NG_009291.1:g.14223_14230del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.901_908del MANE Select	ENSP00000295897.4:p.Glu301Ter
ENST00000295897.8:c.901_908del	ENSP00000295897.4:p.Glu301Ter
ENST00000401494.7:c.556_563del	ENSP00000384695.3:p.Glu186Ter
ENST00000415165.6:c.325_332del	ENSP00000401820.2:p.Glu109Ter
ENST00000476441.6:c.*180_*187del	ENSP00000423727.1:n.*180_*187del
ENST00000484992.1:n.221_228del
ENST00000503124.5:c.451_458del	ENSP00000421027.1:p.Glu151Ter
ENST00000505649.5:n.587_594del
ENST00000509063.5:c.901_908del	ENSP00000422784.1:p.Glu301Ter
ENST00000511370.1:c.434_441del
ENST00000621085.4:c.491-1629_491-1622del	ENSP00000483421.1:n.491-1629_491-1622del
ENST00000621628.4:c.487-1625_487-1618del	ENSP00000480485.1:n.487-1625_487-1618del
NM_000477.5:c.901_908del	NP_000468.1:p.Glu301Ter
NM_000477.6:c.901_908del	NP_000468.1:p.Glu301Ter
NM_000477.7:c.901_908del MANE Select	NP_000468.1:p.Glu301Ter