Canonical Allele Identifier: CA1468141826

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413291T= , CM000666.2:g.73413291T=	GRCh38
NC_000004.11:g.74279008T= , CM000666.1:g.74279008T=	GRCh37
NC_000004.10:g.74497872T=	NCBI36
NG_009291.1:g.14037T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.844-129T= MANE Select	ENSP00000295897.4:n.844-129T=
ENST00000295897.8:c.844-129T=	ENSP00000295897.4:n.844-129T=
ENST00000401494.7:c.499-129T=	ENSP00000384695.3:n.499-129T=
ENST00000415165.6:c.268-129T=	ENSP00000401820.2:n.268-129T=
ENST00000476441.6:c.*123-129T=	ENSP00000423727.1:n.*123-129T=
ENST00000484992.1:n.35T=
ENST00000503124.5:c.394-129T=	ENSP00000421027.1:n.394-129T=
ENST00000505649.5:n.530-129T=
ENST00000509063.5:c.844-129T=	ENSP00000422784.1:n.844-129T=
ENST00000511370.1:c.377-129T=
ENST00000621085.4:c.491-1815T=	ENSP00000483421.1:n.491-1815T=
ENST00000621628.4:c.487-1811T=	ENSP00000480485.1:n.487-1811T=
NM_000477.5:c.844-129T=	NP_000468.1:n.844-129T=
NM_000477.6:c.844-129T=	NP_000468.1:n.844-129T=
NM_000477.7:c.844-129T= MANE Select	NP_000468.1:n.844-129T=