Canonical Allele Identifier: CA357245083

Gene: ALB

Linked Data

• dbSNP Id: rs745553711
• MyVariant Identifiers: chr4:g.74283975C>A (hg19) ; chr4:g.73418258C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418258C>A , CM000666.2:g.73418258C>A	GRCh38
NC_000004.11:g.74283975C>A , CM000666.1:g.74283975C>A	GRCh37
NC_000004.10:g.74502839C>A	NCBI36
NG_009291.1:g.19004C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1599C>A MANE Select	ENSP00000295897.4:p.Phe533Leu
ENST00000295897.8:c.1599C>A	ENSP00000295897.4:p.Phe533Leu
ENST00000401494.7:c.1254C>A	ENSP00000384695.3:p.Phe418Leu
ENST00000415165.6:c.1023C>A	ENSP00000401820.2:p.Phe341Leu
ENST00000476441.6:c.*878C>A	ENSP00000423727.1:n.*878C>A
ENST00000486939.1:n.253C>A
ENST00000503124.5:c.1149C>A	ENSP00000421027.1:p.Phe383Leu
ENST00000505649.5:n.1146C>A
ENST00000509063.5:c.1599C>A	ENSP00000422784.1:p.Phe533Leu
ENST00000511370.1:c.1132C>A
ENST00000621085.4:c.960C>A	ENSP00000483421.1:p.Phe320Leu
ENST00000621628.4:c.960C>A	ENSP00000480485.1:p.Phe320Leu
NM_000477.5:c.1599C>A	NP_000468.1:p.Phe533Leu
NM_000477.6:c.1599C>A	NP_000468.1:p.Phe533Leu
NM_000477.7:c.1599C>A MANE Select	NP_000468.1:p.Phe533Leu