Canonical Allele Identifier: CA1468146614

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418011G= , CM000666.2:g.73418011G=	GRCh38
NC_000004.11:g.74283728G= , CM000666.1:g.74283728G=	GRCh37
NC_000004.10:g.74502592G=	NCBI36
NG_009291.1:g.18757G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1429-77G= MANE Select	ENSP00000295897.4:n.1429-77G=
ENST00000295897.8:c.1429-77G=	ENSP00000295897.4:n.1429-77G=
ENST00000401494.7:c.1084-77G=	ENSP00000384695.3:n.1084-77G=
ENST00000415165.6:c.853-77G=	ENSP00000401820.2:n.853-77G=
ENST00000476441.6:c.*708-77G=	ENSP00000423727.1:n.*708-77G=
ENST00000486939.1:n.6G=
ENST00000503124.5:c.979-77G=	ENSP00000421027.1:n.979-77G=
ENST00000505649.5:n.976-77G=
ENST00000509063.5:c.1429-77G=	ENSP00000422784.1:n.1429-77G=
ENST00000511370.1:c.962-77G=
ENST00000621085.4:c.790-77G=	ENSP00000483421.1:n.790-77G=
ENST00000621628.4:c.790-77G=	ENSP00000480485.1:n.790-77G=
NM_000477.5:c.1429-77G=	NP_000468.1:n.1429-77G=
NM_000477.6:c.1429-77G=	NP_000468.1:n.1429-77G=
NM_000477.7:c.1429-77G= MANE Select	NP_000468.1:n.1429-77G=