Canonical Allele Identifier: CA357244783

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283937T>A (hg19) ; chr4:g.73418220T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418220T>A , CM000666.2:g.73418220T>A	GRCh38
NC_000004.11:g.74283937T>A , CM000666.1:g.74283937T>A	GRCh37
NC_000004.10:g.74502801T>A	NCBI36
NG_009291.1:g.18966T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1561T>A MANE Select	ENSP00000295897.4:p.Tyr521Asn
ENST00000295897.8:c.1561T>A	ENSP00000295897.4:p.Tyr521Asn
ENST00000401494.7:c.1216T>A	ENSP00000384695.3:p.Tyr406Asn
ENST00000415165.6:c.985T>A	ENSP00000401820.2:p.Tyr329Asn
ENST00000476441.6:c.*840T>A	ENSP00000423727.1:n.*840T>A
ENST00000486939.1:n.215T>A
ENST00000503124.5:c.1111T>A	ENSP00000421027.1:p.Tyr371Asn
ENST00000505649.5:n.1108T>A
ENST00000509063.5:c.1561T>A	ENSP00000422784.1:p.Tyr521Asn
ENST00000511370.1:c.1094T>A
ENST00000621085.4:c.922T>A	ENSP00000483421.1:p.Tyr308Asn
ENST00000621628.4:c.922T>A	ENSP00000480485.1:p.Tyr308Asn
NM_000477.5:c.1561T>A	NP_000468.1:p.Tyr521Asn
NM_000477.6:c.1561T>A	NP_000468.1:p.Tyr521Asn
NM_000477.7:c.1561T>A MANE Select	NP_000468.1:p.Tyr521Asn