Canonical Allele Identifier: CA439800346

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280851C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415134C>G , CM000666.2:g.73415134C>G	GRCh38
NC_000004.11:g.74280851C>G , CM000666.1:g.74280851C>G	GRCh37
NC_000004.10:g.74499715C>G	NCBI36
NG_009291.1:g.15880C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1158C>G MANE Select	ENSP00000295897.4:p.Ala386=
ENST00000295897.8:c.1158C>G	ENSP00000295897.4:p.Ala386=
ENST00000401494.7:c.813C>G	ENSP00000384695.3:p.Ala271=
ENST00000415165.6:c.582C>G	ENSP00000401820.2:p.Ala194=
ENST00000476441.6:c.*437C>G	ENSP00000423727.1:n.*437C>G
ENST00000484992.1:n.478C>G
ENST00000503124.5:c.708C>G	ENSP00000421027.1:p.Ala236=
ENST00000504043.1:n.161C>G
ENST00000505649.5:n.844C>G
ENST00000509063.5:c.1158C>G	ENSP00000422784.1:p.Ala386=
ENST00000511370.1:c.691C>G
ENST00000621085.4:c.519C>G	ENSP00000483421.1:p.Ala173=
ENST00000621628.4:c.519C>G	ENSP00000480485.1:p.Ala173=
NM_000477.5:c.1158C>G	NP_000468.1:p.Ala386=
NM_000477.6:c.1158C>G	NP_000468.1:p.Ala386=
NM_000477.7:c.1158C>G MANE Select	NP_000468.1:p.Ala386=