Canonical Allele Identifier: CA1468148698

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420134T= , CM000666.2:g.73420134T=	GRCh38
NC_000004.11:g.74285851T= , CM000666.1:g.74285851T=	GRCh37
NC_000004.10:g.74504715T=	NCBI36
NG_009291.1:g.20880T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-120T= MANE Select	ENSP00000295897.4:n.1786-120T=
ENST00000295897.8:c.1786-120T=	ENSP00000295897.4:n.1786-120T=
ENST00000401494.7:c.1441-120T=	ENSP00000384695.3:n.1441-120T=
ENST00000415165.6:c.1210-120T=	ENSP00000401820.2:n.1210-120T=
ENST00000476441.6:c.*1065-120T=	ENSP00000423727.1:n.*1065-120T=
ENST00000495173.1:n.94-120T=
ENST00000503124.5:c.1336-120T=	ENSP00000421027.1:n.1336-120T=
ENST00000505649.5:n.1333-120T=
ENST00000508932.5:n.176-120T=
ENST00000509063.5:c.1785+495T=	ENSP00000422784.1:n.1785+495T=
ENST00000511370.1:c.1319-120T=
ENST00000621085.4:c.1147-120T=	ENSP00000483421.1:n.1147-120T=
ENST00000621628.4:c.1147-120T=	ENSP00000480485.1:n.1147-120T=
NM_000477.5:c.1786-120T=	NP_000468.1:n.1786-120T=
NM_000477.6:c.1786-120T=	NP_000468.1:n.1786-120T=
NM_000477.7:c.1786-120T= MANE Select	NP_000468.1:n.1786-120T=