Canonical Allele Identifier: CA1468143189

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414772T= , CM000666.2:g.73414772T=	GRCh38
NC_000004.11:g.74280489T= , CM000666.1:g.74280489T=	GRCh37
NC_000004.10:g.74499353T=	NCBI36
NG_009291.1:g.15518T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-263T= MANE Select	ENSP00000295897.4:n.1059-263T=
ENST00000295897.8:c.1059-263T=	ENSP00000295897.4:n.1059-263T=
ENST00000401494.7:c.714-263T=	ENSP00000384695.3:n.714-263T=
ENST00000415165.6:c.483-263T=	ENSP00000401820.2:n.483-263T=
ENST00000476441.6:c.*338-263T=	ENSP00000423727.1:n.*338-263T=
ENST00000484992.1:n.379-263T=
ENST00000503124.5:c.609-263T=	ENSP00000421027.1:n.609-263T=
ENST00000504043.1:n.62-263T=
ENST00000505649.5:n.745-263T=
ENST00000509063.5:c.1059-263T=	ENSP00000422784.1:n.1059-263T=
ENST00000511370.1:c.592-263T=
ENST00000621085.4:c.491-334T=	ENSP00000483421.1:n.491-334T=
ENST00000621628.4:c.487-330T=	ENSP00000480485.1:n.487-330T=
NM_000477.5:c.1059-263T=	NP_000468.1:n.1059-263T=
NM_000477.6:c.1059-263T=	NP_000468.1:n.1059-263T=
NM_000477.7:c.1059-263T= MANE Select	NP_000468.1:n.1059-263T=