Canonical Allele Identifier: CA1468146936

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418253A= , CM000666.2:g.73418253A=	GRCh38
NC_000004.11:g.74283970A= , CM000666.1:g.74283970A=	GRCh37
NC_000004.10:g.74502834A=	NCBI36
NG_009291.1:g.18999A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1594A= MANE Select	ENSP00000295897.4:p.Thr532=
ENST00000295897.8:c.1594A=	ENSP00000295897.4:p.Thr532=
ENST00000401494.7:c.1249A=	ENSP00000384695.3:p.Thr417=
ENST00000415165.6:c.1018A=	ENSP00000401820.2:p.Thr340=
ENST00000476441.6:c.*873A=	ENSP00000423727.1:n.*873A=
ENST00000486939.1:n.248A=
ENST00000503124.5:c.1144A=	ENSP00000421027.1:p.Thr382=
ENST00000505649.5:n.1141A=
ENST00000509063.5:c.1594A=	ENSP00000422784.1:p.Thr532=
ENST00000511370.1:c.1127A=
ENST00000621085.4:c.955A=	ENSP00000483421.1:p.Thr319=
ENST00000621628.4:c.955A=	ENSP00000480485.1:p.Thr319=
NM_000477.5:c.1594A=	NP_000468.1:p.Thr532=
NM_000477.6:c.1594A=	NP_000468.1:p.Thr532=
NM_000477.7:c.1594A= MANE Select	NP_000468.1:p.Thr532=