Canonical Allele Identifier: CA357246705

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285346T>A (hg19) ; chr4:g.73419629T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419629T>A , CM000666.2:g.73419629T>A	GRCh38
NC_000004.11:g.74285346T>A , CM000666.1:g.74285346T>A	GRCh37
NC_000004.10:g.74504210T>A	NCBI36
NG_009291.1:g.20375T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1775T>A MANE Select	ENSP00000295897.4:p.Phe592Tyr
ENST00000295897.8:c.1775T>A	ENSP00000295897.4:p.Phe592Tyr
ENST00000401494.7:c.1430T>A	ENSP00000384695.3:p.Phe477Tyr
ENST00000415165.6:c.1199T>A	ENSP00000401820.2:p.Phe400Tyr
ENST00000476441.6:c.*1054T>A	ENSP00000423727.1:n.*1054T>A
ENST00000495173.1:n.83T>A
ENST00000503124.5:c.1325T>A	ENSP00000421027.1:p.Phe442Tyr
ENST00000505649.5:n.1322T>A
ENST00000508932.5:n.175+174T>A
ENST00000509063.5:c.1775T>A	ENSP00000422784.1:p.Phe592Tyr
ENST00000511370.1:c.1308T>A
ENST00000621085.4:c.1136T>A	ENSP00000483421.1:p.Phe379Tyr
ENST00000621628.4:c.1136T>A	ENSP00000480485.1:p.Phe379Tyr
NM_000477.5:c.1775T>A	NP_000468.1:p.Phe592Tyr
NM_000477.6:c.1775T>A	NP_000468.1:p.Phe592Tyr
NM_000477.7:c.1775T>A MANE Select	NP_000468.1:p.Phe592Tyr