Canonical Allele Identifier: CA357245052

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283970A>G (hg19) ; chr4:g.73418253A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418253A>G , CM000666.2:g.73418253A>G	GRCh38
NC_000004.11:g.74283970A>G , CM000666.1:g.74283970A>G	GRCh37
NC_000004.10:g.74502834A>G	NCBI36
NG_009291.1:g.18999A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1594A>G MANE Select	ENSP00000295897.4:p.Thr532Ala
ENST00000295897.8:c.1594A>G	ENSP00000295897.4:p.Thr532Ala
ENST00000401494.7:c.1249A>G	ENSP00000384695.3:p.Thr417Ala
ENST00000415165.6:c.1018A>G	ENSP00000401820.2:p.Thr340Ala
ENST00000476441.6:c.*873A>G	ENSP00000423727.1:n.*873A>G
ENST00000486939.1:n.248A>G
ENST00000503124.5:c.1144A>G	ENSP00000421027.1:p.Thr382Ala
ENST00000505649.5:n.1141A>G
ENST00000509063.5:c.1594A>G	ENSP00000422784.1:p.Thr532Ala
ENST00000511370.1:c.1127A>G
ENST00000621085.4:c.955A>G	ENSP00000483421.1:p.Thr319Ala
ENST00000621628.4:c.955A>G	ENSP00000480485.1:p.Thr319Ala
NM_000477.5:c.1594A>G	NP_000468.1:p.Thr532Ala
NM_000477.6:c.1594A>G	NP_000468.1:p.Thr532Ala
NM_000477.7:c.1594A>G MANE Select	NP_000468.1:p.Thr532Ala