Canonical Allele Identifier: CA357244306

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283858T>A (hg19) ; chr4:g.73418141T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418141T>A , CM000666.2:g.73418141T>A	GRCh38
NC_000004.11:g.74283858T>A , CM000666.1:g.74283858T>A	GRCh37
NC_000004.10:g.74502722T>A	NCBI36
NG_009291.1:g.18887T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1482T>A MANE Select	ENSP00000295897.4:p.Ser494Arg
ENST00000295897.8:c.1482T>A	ENSP00000295897.4:p.Ser494Arg
ENST00000401494.7:c.1137T>A	ENSP00000384695.3:p.Ser379Arg
ENST00000415165.6:c.906T>A	ENSP00000401820.2:p.Ser302Arg
ENST00000476441.6:c.*761T>A	ENSP00000423727.1:n.*761T>A
ENST00000486939.1:n.136T>A
ENST00000503124.5:c.1032T>A	ENSP00000421027.1:p.Ser344Arg
ENST00000505649.5:n.1029T>A
ENST00000509063.5:c.1482T>A	ENSP00000422784.1:p.Ser494Arg
ENST00000511370.1:c.1015T>A
ENST00000621085.4:c.843T>A	ENSP00000483421.1:p.Ser281Arg
ENST00000621628.4:c.843T>A	ENSP00000480485.1:p.Ser281Arg
NM_000477.5:c.1482T>A	NP_000468.1:p.Ser494Arg
NM_000477.6:c.1482T>A	NP_000468.1:p.Ser494Arg
NM_000477.7:c.1482T>A MANE Select	NP_000468.1:p.Ser494Arg