Canonical Allele Identifier: CA1468148906

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420313G= , CM000666.2:g.73420313G=	GRCh38
NC_000004.11:g.74286030G= , CM000666.1:g.74286030G=	GRCh37
NC_000004.10:g.74504894G=	NCBI36
NG_009291.1:g.21059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*15G= MANE Select	ENSP00000295897.4:n.*15G=
ENST00000295897.8:c.*15G=	ENSP00000295897.4:n.*15G=
ENST00000401494.7:c.*15G=	ENSP00000384695.3:n.*15G=
ENST00000415165.6:c.*15G=	ENSP00000401820.2:n.*15G=
ENST00000476441.6:c.*1124G=	ENSP00000423727.1:n.*1124G=
ENST00000495173.1:n.153G=
ENST00000503124.5:c.*15G=	ENSP00000421027.1:n.*15G=
ENST00000505649.5:n.1392G=
ENST00000508932.5:n.235G=
ENST00000509063.5:c.1785+674G=	ENSP00000422784.1:n.1785+674G=
ENST00000511370.1:c.1378G=
ENST00000621085.4:c.*15G=	ENSP00000483421.1:n.*15G=
ENST00000621628.4:c.*15G=	ENSP00000480485.1:n.*15G=
NM_000477.5:c.*15G=	NP_000468.1:n.*15G=
NM_000477.6:c.*15G=	NP_000468.1:n.*15G=
NM_000477.7:c.*15G= MANE Select	NP_000468.1:n.*15G=