Canonical Allele Identifier: CA1468152312

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408604T= , CM000666.2:g.73408604T=	GRCh38
NC_000004.11:g.74274321T= , CM000666.1:g.74274321T=	GRCh37
NC_000004.10:g.74493185T=	NCBI36
NG_009291.1:g.9350T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.281T= MANE Select	ENSP00000295897.4:p.Phe94=
ENST00000295897.8:c.281T=	ENSP00000295897.4:p.Phe94=
ENST00000401494.7:c.138-751T=	ENSP00000384695.3:n.138-751T=
ENST00000415165.6:c.138-3392T=	ENSP00000401820.2:n.138-3392T=
ENST00000441319.5:c.287T=	ENSP00000392541.1:p.Phe96=
ENST00000476441.6:c.80-751T=	ENSP00000423727.1:n.80-751T=
ENST00000503124.5:c.33-751T=	ENSP00000421027.1:n.33-751T=
ENST00000509063.5:c.281T=	ENSP00000422784.1:p.Phe94=
ENST00000510166.5:n.317T=
ENST00000514786.1:n.250T=
ENST00000515133.5:n.322T=
ENST00000621085.4:c.281T=	ENSP00000483421.1:p.Phe94=
ENST00000621628.4:c.281T=	ENSP00000480485.1:p.Phe94=
NM_000477.5:c.281T=	NP_000468.1:p.Phe94=
NM_000477.6:c.281T=	NP_000468.1:p.Phe94=
NM_000477.7:c.281T= MANE Select	NP_000468.1:p.Phe94=