Canonical Allele Identifier: CA357247192

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285994T>G (hg19) ; chr4:g.73420277T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420277T>G , CM000666.2:g.73420277T>G	GRCh38
NC_000004.11:g.74285994T>G , CM000666.1:g.74285994T>G	GRCh37
NC_000004.10:g.74504858T>G	NCBI36
NG_009291.1:g.21023T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1809T>G MANE Select	ENSP00000295897.4:p.Ser603Arg
ENST00000295897.8:c.1809T>G	ENSP00000295897.4:p.Ser603Arg
ENST00000401494.7:c.1464T>G	ENSP00000384695.3:p.Ser488Arg
ENST00000415165.6:c.1233T>G	ENSP00000401820.2:p.Ser411Arg
ENST00000476441.6:c.*1088T>G	ENSP00000423727.1:n.*1088T>G
ENST00000495173.1:n.117T>G
ENST00000503124.5:c.1359T>G	ENSP00000421027.1:p.Ser453Arg
ENST00000505649.5:n.1356T>G
ENST00000508932.5:n.199T>G
ENST00000509063.5:c.1785+638T>G	ENSP00000422784.1:n.1785+638T>G
ENST00000511370.1:c.1342T>G
ENST00000621085.4:c.1170T>G	ENSP00000483421.1:p.Ser390Arg
ENST00000621628.4:c.1170T>G	ENSP00000480485.1:p.Ser390Arg
NM_000477.5:c.1809T>G	NP_000468.1:p.Ser603Arg
NM_000477.6:c.1809T>G	NP_000468.1:p.Ser603Arg
NM_000477.7:c.1809T>G MANE Select	NP_000468.1:p.Ser603Arg