Canonical Allele Identifier: CA357244800

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283939C>A (hg19) ; chr4:g.73418222C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418222C>A , CM000666.2:g.73418222C>A	GRCh38
NC_000004.11:g.74283939C>A , CM000666.1:g.74283939C>A	GRCh37
NC_000004.10:g.74502803C>A	NCBI36
NG_009291.1:g.18968C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1563C>A MANE Select	ENSP00000295897.4:p.Tyr521Ter
ENST00000295897.8:c.1563C>A	ENSP00000295897.4:p.Tyr521Ter
ENST00000401494.7:c.1218C>A	ENSP00000384695.3:p.Tyr406Ter
ENST00000415165.6:c.987C>A	ENSP00000401820.2:p.Tyr329Ter
ENST00000476441.6:c.*842C>A	ENSP00000423727.1:n.*842C>A
ENST00000486939.1:n.217C>A
ENST00000503124.5:c.1113C>A	ENSP00000421027.1:p.Tyr371Ter
ENST00000505649.5:n.1110C>A
ENST00000509063.5:c.1563C>A	ENSP00000422784.1:p.Tyr521Ter
ENST00000511370.1:c.1096C>A
ENST00000621085.4:c.924C>A	ENSP00000483421.1:p.Tyr308Ter
ENST00000621628.4:c.924C>A	ENSP00000480485.1:p.Tyr308Ter
NM_000477.5:c.1563C>A	NP_000468.1:p.Tyr521Ter
NM_000477.6:c.1563C>A	NP_000468.1:p.Tyr521Ter
NM_000477.7:c.1563C>A MANE Select	NP_000468.1:p.Tyr521Ter