Canonical Allele Identifier: CA1468148871

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420279A= , CM000666.2:g.73420279A=	GRCh38
NC_000004.11:g.74285996A= , CM000666.1:g.74285996A=	GRCh37
NC_000004.10:g.74504860A=	NCBI36
NG_009291.1:g.21025A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1811A= MANE Select	ENSP00000295897.4:p.Gln604=
ENST00000295897.8:c.1811A=	ENSP00000295897.4:p.Gln604=
ENST00000401494.7:c.1466A=	ENSP00000384695.3:p.Gln489=
ENST00000415165.6:c.1235A=	ENSP00000401820.2:p.Gln412=
ENST00000476441.6:c.*1090A=	ENSP00000423727.1:n.*1090A=
ENST00000495173.1:n.119A=
ENST00000503124.5:c.1361A=	ENSP00000421027.1:p.Gln454=
ENST00000505649.5:n.1358A=
ENST00000508932.5:n.201A=
ENST00000509063.5:c.1785+640A=	ENSP00000422784.1:n.1785+640A=
ENST00000511370.1:c.1344A=
ENST00000621085.4:c.1172A=	ENSP00000483421.1:p.Gln391=
ENST00000621628.4:c.1172A=	ENSP00000480485.1:p.Gln391=
NM_000477.5:c.1811A=	NP_000468.1:p.Gln604=
NM_000477.6:c.1811A=	NP_000468.1:p.Gln604=
NM_000477.7:c.1811A= MANE Select	NP_000468.1:p.Gln604=