Canonical Allele Identifier: CA99701063

Gene: ALB

Linked Data

• dbSNP Id: rs55764359
• gnomAD v2: 4-74274864-G-GCACA
• gnomAD v3: 4-73409147-G-GCACA
• gnomAD v4: 4-73409147-G-GCACA
• MyVariant Identifiers: chr4:g.74274889_74274890insACAC (hg19) ; chr4:g.74274868_74274869insCACA (hg19) ; chr4:g.74274864_74274865insCACA (hg19) ; chr4:g.73409172_73409173insACAC (hg38) ; chr4:g.73409151_73409152insCACA (hg38) ; chr4:g.73409147_73409148insCACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409169_73409172dup , CM000666.2:g.73409169_73409172dup	GRCh38
NC_000004.11:g.74274886_74274889dup , CM000666.1:g.74274886_74274889dup	GRCh37
NC_000004.10:g.74493750_74493753dup	NCBI36
NG_009291.1:g.9915_9918dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-186_483-183dup MANE Select	ENSP00000295897.4:n.483-186_483-183dup
ENST00000295897.8:c.483-186_483-183dup	ENSP00000295897.4:n.483-186_483-183dup
ENST00000401494.7:c.138-186_138-183dup	ENSP00000384695.3:n.138-186_138-183dup
ENST00000415165.6:c.138-2827_138-2824dup	ENSP00000401820.2:n.138-2827_138-2824dup
ENST00000441319.5:c.489-186_489-183dup	ENSP00000392541.1:n.489-186_489-183dup
ENST00000476441.6:c.80-186_80-183dup	ENSP00000423727.1:n.80-186_80-183dup
ENST00000503124.5:c.33-186_33-183dup	ENSP00000421027.1:n.33-186_33-183dup
ENST00000505649.5:n.169-186_169-183dup
ENST00000509063.5:c.483-186_483-183dup	ENSP00000422784.1:n.483-186_483-183dup
ENST00000514786.1:n.452-186_452-183dup
ENST00000621085.4:c.483-186_483-183dup	ENSP00000483421.1:n.483-186_483-183dup
ENST00000621628.4:c.486+93_486+96dup	ENSP00000480485.1:n.486+93_486+96dup
NM_000477.5:c.483-186_483-183dup	NP_000468.1:n.483-186_483-183dup
NM_000477.6:c.483-186_483-183dup	NP_000468.1:n.483-186_483-183dup
NM_000477.7:c.483-186_483-183dup MANE Select	NP_000468.1:n.483-186_483-183dup