Canonical Allele Identifier: CA99698128

Gene: ALB

Linked Data

• dbSNP Id: rs1015417165
• gnomAD v2: 4-74271969-C-CT
• gnomAD v3: 4-73406252-C-CT
• gnomAD v4: 4-73406252-C-CT
• MyVariant Identifiers: chr4:g.74271969_74271970insT (hg19) ; chr4:g.73406252_73406253insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406253dup , CM000666.2:g.73406253dup	GRCh38
NC_000004.11:g.74271970dup , CM000666.1:g.74271970dup	GRCh37
NC_000004.10:g.74490834dup	NCBI36
NG_009291.1:g.6999dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-376dup MANE Select	ENSP00000295897.4:n.138-376dup
ENST00000295897.8:c.138-376dup	ENSP00000295897.4:n.138-376dup
ENST00000401494.7:c.137+1080dup	ENSP00000384695.3:n.137+1080dup
ENST00000415165.6:c.137+1080dup	ENSP00000401820.2:n.137+1080dup
ENST00000441319.5:c.144-376dup	ENSP00000392541.1:n.144-376dup
ENST00000476441.6:c.79+1847dup	ENSP00000423727.1:n.79+1847dup
ENST00000503124.5:c.-101-376dup	ENSP00000421027.1:n.-101-376dup
ENST00000509063.5:c.138-376dup	ENSP00000422784.1:n.138-376dup
ENST00000510166.5:n.174-376dup
ENST00000514786.1:n.107-376dup
ENST00000515133.5:n.179-376dup
ENST00000621085.4:c.138-376dup	ENSP00000483421.1:n.138-376dup
ENST00000621628.4:c.138-376dup	ENSP00000480485.1:n.138-376dup
NM_000477.5:c.138-376dup	NP_000468.1:n.138-376dup
NM_000477.6:c.138-376dup	NP_000468.1:n.138-376dup
NM_000477.7:c.138-376dup MANE Select	NP_000468.1:n.138-376dup