Canonical Allele Identifier: CA552304914

Gene: ALB

Linked Data

• dbSNP Id: rs1449563577
• gnomAD v2: 4-74272444-CTGA-C
• gnomAD v4: 4-73406727-CTGA-C
• MyVariant Identifiers: chr4:g.74272445_74272447del (hg19) ; chr4:g.73406728_73406730del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406731_73406733del , CM000666.2:g.73406731_73406733del	GRCh38
NC_000004.11:g.74272448_74272450del , CM000666.1:g.74272448_74272450del	GRCh37
NC_000004.10:g.74491312_74491314del	NCBI36
NG_009291.1:g.7477_7479del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.240_242del MANE Select	ENSP00000295897.4:p.Asp80del
ENST00000295897.8:c.240_242del	ENSP00000295897.4:p.Asp80del
ENST00000401494.7:c.137+1558_137+1560del	ENSP00000384695.3:n.137+1558_137+1560del
ENST00000415165.6:c.137+1558_137+1560del	ENSP00000401820.2:n.137+1558_137+1560del
ENST00000441319.5:c.246_248del	ENSP00000392541.1:p.Asp82del
ENST00000476441.6:c.79+2325_79+2327del	ENSP00000423727.1:n.79+2325_79+2327del
ENST00000503124.5:c.2_4del	ENSP00000421027.1:p.Met1del
ENST00000509063.5:c.240_242del	ENSP00000422784.1:p.Asp80del
ENST00000510166.5:n.276_278del
ENST00000514786.1:n.209_211del
ENST00000515133.5:n.281_283del
ENST00000621085.4:c.240_242del	ENSP00000483421.1:p.Asp80del
ENST00000621628.4:c.240_242del	ENSP00000480485.1:p.Asp80del
NM_000477.5:c.240_242del	NP_000468.1:p.Asp80del
NM_000477.6:c.240_242del	NP_000468.1:p.Asp80del
NM_000477.7:c.240_242del MANE Select	NP_000468.1:p.Asp80del