Canonical Allele Identifier: CA357244472

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283886T>G (hg19) ; chr4:g.73418169T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418169T>G , CM000666.2:g.73418169T>G	GRCh38
NC_000004.11:g.74283886T>G , CM000666.1:g.74283886T>G	GRCh37
NC_000004.10:g.74502750T>G	NCBI36
NG_009291.1:g.18915T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1510T>G MANE Select	ENSP00000295897.4:p.Ser504Ala
ENST00000295897.8:c.1510T>G	ENSP00000295897.4:p.Ser504Ala
ENST00000401494.7:c.1165T>G	ENSP00000384695.3:p.Ser389Ala
ENST00000415165.6:c.934T>G	ENSP00000401820.2:p.Ser312Ala
ENST00000476441.6:c.*789T>G	ENSP00000423727.1:n.*789T>G
ENST00000486939.1:n.164T>G
ENST00000503124.5:c.1060T>G	ENSP00000421027.1:p.Ser354Ala
ENST00000505649.5:n.1057T>G
ENST00000509063.5:c.1510T>G	ENSP00000422784.1:p.Ser504Ala
ENST00000511370.1:c.1043T>G
ENST00000621085.4:c.871T>G	ENSP00000483421.1:p.Ser291Ala
ENST00000621628.4:c.871T>G	ENSP00000480485.1:p.Ser291Ala
NM_000477.5:c.1510T>G	NP_000468.1:p.Ser504Ala
NM_000477.6:c.1510T>G	NP_000468.1:p.Ser504Ala
NM_000477.7:c.1510T>G MANE Select	NP_000468.1:p.Ser504Ala