Canonical Allele Identifier: CA439800349

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280854T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415137T>G , CM000666.2:g.73415137T>G	GRCh38
NC_000004.11:g.74280854T>G , CM000666.1:g.74280854T>G	GRCh37
NC_000004.10:g.74499718T>G	NCBI36
NG_009291.1:g.15883T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1161T>G MANE Select	ENSP00000295897.4:p.Ala387=
ENST00000295897.8:c.1161T>G	ENSP00000295897.4:p.Ala387=
ENST00000401494.7:c.816T>G	ENSP00000384695.3:p.Ala272=
ENST00000415165.6:c.585T>G	ENSP00000401820.2:p.Ala195=
ENST00000476441.6:c.*440T>G	ENSP00000423727.1:n.*440T>G
ENST00000484992.1:n.481T>G
ENST00000503124.5:c.711T>G	ENSP00000421027.1:p.Ala237=
ENST00000504043.1:n.164T>G
ENST00000505649.5:n.847T>G
ENST00000509063.5:c.1161T>G	ENSP00000422784.1:p.Ala387=
ENST00000511370.1:c.694T>G
ENST00000621085.4:c.522T>G	ENSP00000483421.1:p.Ala174=
ENST00000621628.4:c.522T>G	ENSP00000480485.1:p.Ala174=
NM_000477.5:c.1161T>G	NP_000468.1:p.Ala387=
NM_000477.6:c.1161T>G	NP_000468.1:p.Ala387=
NM_000477.7:c.1161T>G MANE Select	NP_000468.1:p.Ala387=