Canonical Allele Identifier: CA1468150656

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406443G= , CM000666.2:g.73406443G=	GRCh38
NC_000004.11:g.74272160G= , CM000666.1:g.74272160G=	GRCh37
NC_000004.10:g.74491024G=	NCBI36
NG_009291.1:g.7189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-186G= MANE Select	ENSP00000295897.4:n.138-186G=
ENST00000295897.8:c.138-186G=	ENSP00000295897.4:n.138-186G=
ENST00000401494.7:c.137+1270G=	ENSP00000384695.3:n.137+1270G=
ENST00000415165.6:c.137+1270G=	ENSP00000401820.2:n.137+1270G=
ENST00000441319.5:c.144-186G=	ENSP00000392541.1:n.144-186G=
ENST00000476441.6:c.79+2037G=	ENSP00000423727.1:n.79+2037G=
ENST00000503124.5:c.-101-186G=	ENSP00000421027.1:n.-101-186G=
ENST00000509063.5:c.138-186G=	ENSP00000422784.1:n.138-186G=
ENST00000510166.5:n.174-186G=
ENST00000514786.1:n.107-186G=
ENST00000515133.5:n.179-186G=
ENST00000621085.4:c.138-186G=	ENSP00000483421.1:n.138-186G=
ENST00000621628.4:c.138-186G=	ENSP00000480485.1:n.138-186G=
NM_000477.5:c.138-186G=	NP_000468.1:n.138-186G=
NM_000477.6:c.138-186G=	NP_000468.1:n.138-186G=
NM_000477.7:c.138-186G= MANE Select	NP_000468.1:n.138-186G=