Canonical Allele Identifier: CA439801119

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286015A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420298A>G , CM000666.2:g.73420298A>G	GRCh38
NC_000004.11:g.74286015A>G , CM000666.1:g.74286015A>G	GRCh37
NC_000004.10:g.74504879A>G	NCBI36
NG_009291.1:g.21044A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1830A>G MANE Select	ENSP00000295897.4:p.Ter610=
ENST00000295897.8:c.1830A>G	ENSP00000295897.4:p.Ter610=
ENST00000401494.7:c.1485A>G	ENSP00000384695.3:p.Ter495=
ENST00000415165.6:c.1254A>G	ENSP00000401820.2:p.Ter418=
ENST00000476441.6:c.*1109A>G	ENSP00000423727.1:n.*1109A>G
ENST00000495173.1:n.138A>G
ENST00000503124.5:c.1380A>G	ENSP00000421027.1:p.Ter460=
ENST00000505649.5:n.1377A>G
ENST00000508932.5:n.220A>G
ENST00000509063.5:c.1785+659A>G	ENSP00000422784.1:n.1785+659A>G
ENST00000511370.1:c.1363A>G
ENST00000621085.4:c.1191A>G	ENSP00000483421.1:p.Ter397=
ENST00000621628.4:c.1191A>G	ENSP00000480485.1:p.Ter397=
NM_000477.5:c.1830A>G	NP_000468.1:p.Ter610=
NM_000477.6:c.1830A>G	NP_000468.1:p.Ter610=
NM_000477.7:c.1830A>G MANE Select	NP_000468.1:p.Ter610=