Canonical Allele Identifier: CA357244443

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283880A>G (hg19) ; chr4:g.73418163A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418163A>G , CM000666.2:g.73418163A>G	GRCh38
NC_000004.11:g.74283880A>G , CM000666.1:g.74283880A>G	GRCh37
NC_000004.10:g.74502744A>G	NCBI36
NG_009291.1:g.18909A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1504A>G MANE Select	ENSP00000295897.4:p.Thr502Ala
ENST00000295897.8:c.1504A>G	ENSP00000295897.4:p.Thr502Ala
ENST00000401494.7:c.1159A>G	ENSP00000384695.3:p.Thr387Ala
ENST00000415165.6:c.928A>G	ENSP00000401820.2:p.Thr310Ala
ENST00000476441.6:c.*783A>G	ENSP00000423727.1:n.*783A>G
ENST00000486939.1:n.158A>G
ENST00000503124.5:c.1054A>G	ENSP00000421027.1:p.Thr352Ala
ENST00000505649.5:n.1051A>G
ENST00000509063.5:c.1504A>G	ENSP00000422784.1:p.Thr502Ala
ENST00000511370.1:c.1037A>G
ENST00000621085.4:c.865A>G	ENSP00000483421.1:p.Thr289Ala
ENST00000621628.4:c.865A>G	ENSP00000480485.1:p.Thr289Ala
NM_000477.5:c.1504A>G	NP_000468.1:p.Thr502Ala
NM_000477.6:c.1504A>G	NP_000468.1:p.Thr502Ala
NM_000477.7:c.1504A>G MANE Select	NP_000468.1:p.Thr502Ala