Canonical Allele Identifier: CA357244788

Gene: ALB

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1561T>G MANE Select	ENSP00000295897.4:p.Tyr521Asp
ENST00000295897.8:c.1561T>G	ENSP00000295897.4:p.Tyr521Asp
ENST00000401494.7:c.1216T>G	ENSP00000384695.3:p.Tyr406Asp
ENST00000415165.6:c.985T>G	ENSP00000401820.2:p.Tyr329Asp
ENST00000476441.6:c.*840T>G	ENSP00000423727.1:n.*840T>G
ENST00000486939.1:n.215T>G
ENST00000503124.5:c.1111T>G	ENSP00000421027.1:p.Tyr371Asp
ENST00000505649.5:n.1108T>G
ENST00000509063.5:c.1561T>G	ENSP00000422784.1:p.Tyr521Asp
ENST00000511370.1:c.1094T>G
ENST00000621085.4:c.922T>G	ENSP00000483421.1:p.Tyr308Asp
ENST00000621628.4:c.922T>G	ENSP00000480485.1:p.Tyr308Asp
NM_000477.5:c.1561T>G	NP_000468.1:p.Tyr521Asp
NM_000477.6:c.1561T>G	NP_000468.1:p.Tyr521Asp
NM_000477.7:c.1561T>G MANE Select	NP_000468.1:p.Tyr521Asp