Canonical Allele Identifier: CA798292377

Gene: ALB

Linked Data

• dbSNP Id: rs1274226966
• gnomAD v3: 4-73418144-C-CA
• gnomAD v4: 4-73418144-C-CA
• MyVariant Identifiers: chr4:g.74283861_74283862insA (hg19) ; chr4:g.73418144_73418145insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418145dup , CM000666.2:g.73418145dup	GRCh38
NC_000004.11:g.74283862dup , CM000666.1:g.74283862dup	GRCh37
NC_000004.10:g.74502726dup	NCBI36
NG_009291.1:g.18891dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1486dup MANE Select	ENSP00000295897.4:p.Arg496LysfsTer24
ENST00000295897.8:c.1486dup	ENSP00000295897.4:p.Arg496LysfsTer24
ENST00000401494.7:c.1141dup	ENSP00000384695.3:p.Arg381LysfsTer24
ENST00000415165.6:c.910dup	ENSP00000401820.2:p.Arg304LysfsTer24
ENST00000476441.6:c.*765dup	ENSP00000423727.1:n.*765dup
ENST00000486939.1:n.140dup
ENST00000503124.5:c.1036dup	ENSP00000421027.1:p.Arg346LysfsTer24
ENST00000505649.5:n.1033dup
ENST00000509063.5:c.1486dup	ENSP00000422784.1:p.Arg496LysfsTer24
ENST00000511370.1:c.1019dup
ENST00000621085.4:c.847dup	ENSP00000483421.1:p.Arg283LysfsTer24
ENST00000621628.4:c.847dup	ENSP00000480485.1:p.Arg283LysfsTer24
NM_000477.5:c.1486dup	NP_000468.1:p.Arg496LysfsTer24
NM_000477.6:c.1486dup	NP_000468.1:p.Arg496LysfsTer24
NM_000477.7:c.1486dup MANE Select	NP_000468.1:p.Arg496LysfsTer24