Canonical Allele Identifier: CA439801113

Gene: ALB

Linked Data

• COSMIC: COSM4799152
• MyVariant Identifiers: chr4:g.74286009C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420292C>T , CM000666.2:g.73420292C>T	GRCh38
NC_000004.11:g.74286009C>T , CM000666.1:g.74286009C>T	GRCh37
NC_000004.10:g.74504873C>T	NCBI36
NG_009291.1:g.21038C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1824C>T MANE Select	ENSP00000295897.4:p.Gly608=
ENST00000295897.8:c.1824C>T	ENSP00000295897.4:p.Gly608=
ENST00000401494.7:c.1479C>T	ENSP00000384695.3:p.Gly493=
ENST00000415165.6:c.1248C>T	ENSP00000401820.2:p.Gly416=
ENST00000476441.6:c.*1103C>T	ENSP00000423727.1:n.*1103C>T
ENST00000495173.1:n.132C>T
ENST00000503124.5:c.1374C>T	ENSP00000421027.1:p.Gly458=
ENST00000505649.5:n.1371C>T
ENST00000508932.5:n.214C>T
ENST00000509063.5:c.1785+653C>T	ENSP00000422784.1:n.1785+653C>T
ENST00000511370.1:c.1357C>T
ENST00000621085.4:c.1185C>T	ENSP00000483421.1:p.Gly395=
ENST00000621628.4:c.1185C>T	ENSP00000480485.1:p.Gly395=
NM_000477.5:c.1824C>T	NP_000468.1:p.Gly608=
NM_000477.6:c.1824C>T	NP_000468.1:p.Gly608=
NM_000477.7:c.1824C>T MANE Select	NP_000468.1:p.Gly608=