Canonical Allele Identifier: CA1468152287

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408537T= , CM000666.2:g.73408537T=	GRCh38
NC_000004.11:g.74274254T= , CM000666.1:g.74274254T=	GRCh37
NC_000004.10:g.74493118T=	NCBI36
NG_009291.1:g.9283T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.271-57T= MANE Select	ENSP00000295897.4:n.271-57T=
ENST00000295897.8:c.271-57T=	ENSP00000295897.4:n.271-57T=
ENST00000401494.7:c.138-818T=	ENSP00000384695.3:n.138-818T=
ENST00000415165.6:c.137+3364T=	ENSP00000401820.2:n.137+3364T=
ENST00000441319.5:c.277-57T=	ENSP00000392541.1:n.277-57T=
ENST00000476441.6:c.80-818T=	ENSP00000423727.1:n.80-818T=
ENST00000503124.5:c.33-818T=	ENSP00000421027.1:n.33-818T=
ENST00000509063.5:c.271-57T=	ENSP00000422784.1:n.271-57T=
ENST00000510166.5:n.307-57T=
ENST00000514786.1:n.240-57T=
ENST00000515133.5:n.312-57T=
ENST00000621085.4:c.271-57T=	ENSP00000483421.1:n.271-57T=
ENST00000621628.4:c.271-57T=	ENSP00000480485.1:n.271-57T=
NM_000477.5:c.271-57T=	NP_000468.1:n.271-57T=
NM_000477.6:c.271-57T=	NP_000468.1:n.271-57T=
NM_000477.7:c.271-57T= MANE Select	NP_000468.1:n.271-57T=