Canonical Allele Identifier: CA439800311

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280815C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415098C>G , CM000666.2:g.73415098C>G	GRCh38
NC_000004.11:g.74280815C>G , CM000666.1:g.74280815C>G	GRCh37
NC_000004.10:g.74499679C>G	NCBI36
NG_009291.1:g.15844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1122C>G MANE Select	ENSP00000295897.4:p.Ala374=
ENST00000295897.8:c.1122C>G	ENSP00000295897.4:p.Ala374=
ENST00000401494.7:c.777C>G	ENSP00000384695.3:p.Ala259=
ENST00000415165.6:c.546C>G	ENSP00000401820.2:p.Ala182=
ENST00000476441.6:c.*401C>G	ENSP00000423727.1:n.*401C>G
ENST00000484992.1:n.442C>G
ENST00000503124.5:c.672C>G	ENSP00000421027.1:p.Ala224=
ENST00000504043.1:n.125C>G
ENST00000505649.5:n.808C>G
ENST00000509063.5:c.1122C>G	ENSP00000422784.1:p.Ala374=
ENST00000511370.1:c.655C>G
ENST00000621085.4:c.491-8C>G	ENSP00000483421.1:n.491-8C>G
ENST00000621628.4:c.487-4C>G	ENSP00000480485.1:n.487-4C>G
NM_000477.5:c.1122C>G	NP_000468.1:p.Ala374=
NM_000477.6:c.1122C>G	NP_000468.1:p.Ala374=
NM_000477.7:c.1122C>G MANE Select	NP_000468.1:p.Ala374=