Canonical Allele Identifier: CA1468141793

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413259C= , CM000666.2:g.73413259C=	GRCh38
NC_000004.11:g.74278976C= , CM000666.1:g.74278976C=	GRCh37
NC_000004.10:g.74497840C=	NCBI36
NG_009291.1:g.14005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.844-161C= MANE Select	ENSP00000295897.4:n.844-161C=
ENST00000295897.8:c.844-161C=	ENSP00000295897.4:n.844-161C=
ENST00000401494.7:c.499-161C=	ENSP00000384695.3:n.499-161C=
ENST00000415165.6:c.268-161C=	ENSP00000401820.2:n.268-161C=
ENST00000476441.6:c.*123-161C=	ENSP00000423727.1:n.*123-161C=
ENST00000484992.1:n.3C=
ENST00000503124.5:c.394-161C=	ENSP00000421027.1:n.394-161C=
ENST00000505649.5:n.530-161C=
ENST00000509063.5:c.844-161C=	ENSP00000422784.1:n.844-161C=
ENST00000511370.1:c.377-161C=
ENST00000621085.4:c.491-1847C=	ENSP00000483421.1:n.491-1847C=
ENST00000621628.4:c.487-1843C=	ENSP00000480485.1:n.487-1843C=
NM_000477.5:c.844-161C=	NP_000468.1:n.844-161C=
NM_000477.6:c.844-161C=	NP_000468.1:n.844-161C=
NM_000477.7:c.844-161C= MANE Select	NP_000468.1:n.844-161C=