Canonical Allele Identifier: CA357244282

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283853G>A (hg19) ; chr4:g.73418136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418136G>A , CM000666.2:g.73418136G>A	GRCh38
NC_000004.11:g.74283853G>A , CM000666.1:g.74283853G>A	GRCh37
NC_000004.10:g.74502717G>A	NCBI36
NG_009291.1:g.18882G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1477G>A MANE Select	ENSP00000295897.4:p.Val493Ile
ENST00000295897.8:c.1477G>A	ENSP00000295897.4:p.Val493Ile
ENST00000401494.7:c.1132G>A	ENSP00000384695.3:p.Val378Ile
ENST00000415165.6:c.901G>A	ENSP00000401820.2:p.Val301Ile
ENST00000476441.6:c.*756G>A	ENSP00000423727.1:n.*756G>A
ENST00000486939.1:n.131G>A
ENST00000503124.5:c.1027G>A	ENSP00000421027.1:p.Val343Ile
ENST00000505649.5:n.1024G>A
ENST00000509063.5:c.1477G>A	ENSP00000422784.1:p.Val493Ile
ENST00000511370.1:c.1010G>A
ENST00000621085.4:c.838G>A	ENSP00000483421.1:p.Val280Ile
ENST00000621628.4:c.838G>A	ENSP00000480485.1:p.Val280Ile
NM_000477.5:c.1477G>A	NP_000468.1:p.Val493Ile
NM_000477.6:c.1477G>A	NP_000468.1:p.Val493Ile
NM_000477.7:c.1477G>A MANE Select	NP_000468.1:p.Val493Ile