Canonical Allele Identifier: CA1468143611

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415142A= , CM000666.2:g.73415142A=	GRCh38
NC_000004.11:g.74280859A= , CM000666.1:g.74280859A=	GRCh37
NC_000004.10:g.74499723A=	NCBI36
NG_009291.1:g.15888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1166A= MANE Select	ENSP00000295897.4:p.Asp389=
ENST00000295897.8:c.1166A=	ENSP00000295897.4:p.Asp389=
ENST00000401494.7:c.821A=	ENSP00000384695.3:p.Asp274=
ENST00000415165.6:c.590A=	ENSP00000401820.2:p.Asp197=
ENST00000476441.6:c.*445A=	ENSP00000423727.1:n.*445A=
ENST00000484992.1:n.486A=
ENST00000503124.5:c.716A=	ENSP00000421027.1:p.Asp239=
ENST00000504043.1:n.169A=
ENST00000505649.5:n.852A=
ENST00000509063.5:c.1166A=	ENSP00000422784.1:p.Asp389=
ENST00000511370.1:c.699A=
ENST00000621085.4:c.527A=	ENSP00000483421.1:p.Asp176=
ENST00000621628.4:c.527A=	ENSP00000480485.1:p.Asp176=
NM_000477.5:c.1166A=	NP_000468.1:p.Asp389=
NM_000477.6:c.1166A=	NP_000468.1:p.Asp389=
NM_000477.7:c.1166A= MANE Select	NP_000468.1:p.Asp389=