Canonical Allele Identifier: CA798290422

Gene: ALB

Linked Data

• dbSNP Id: rs1284184957
• gnomAD v3: 4-73414982-A-AT
• gnomAD v4: 4-73414982-A-AT
• MyVariant Identifiers: chr4:g.74280699_74280700insT (hg19) ; chr4:g.73414982_73414983insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414988dup , CM000666.2:g.73414988dup	GRCh38
NC_000004.11:g.74280705dup , CM000666.1:g.74280705dup	GRCh37
NC_000004.10:g.74499569dup	NCBI36
NG_009291.1:g.15734dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059-47dup MANE Select	ENSP00000295897.4:n.1059-47dup
ENST00000295897.8:c.1059-47dup	ENSP00000295897.4:n.1059-47dup
ENST00000401494.7:c.714-47dup	ENSP00000384695.3:n.714-47dup
ENST00000415165.6:c.483-47dup	ENSP00000401820.2:n.483-47dup
ENST00000476441.6:c.*338-47dup	ENSP00000423727.1:n.*338-47dup
ENST00000484992.1:n.379-47dup
ENST00000503124.5:c.609-47dup	ENSP00000421027.1:n.609-47dup
ENST00000504043.1:n.62-47dup
ENST00000505649.5:n.745-47dup
ENST00000509063.5:c.1059-47dup	ENSP00000422784.1:n.1059-47dup
ENST00000511370.1:c.592-47dup
ENST00000621085.4:c.491-118dup	ENSP00000483421.1:n.491-118dup
ENST00000621628.4:c.487-114dup	ENSP00000480485.1:n.487-114dup
NM_000477.5:c.1059-47dup	NP_000468.1:n.1059-47dup
NM_000477.6:c.1059-47dup	NP_000468.1:n.1059-47dup
NM_000477.7:c.1059-47dup MANE Select	NP_000468.1:n.1059-47dup