Canonical Allele Identifier: CA1468149097

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420499T= , CM000666.2:g.73420499T=	GRCh38
NC_000004.11:g.74286216T= , CM000666.1:g.74286216T=	GRCh37
NC_000004.10:g.74505080T=	NCBI36
NG_009291.1:g.21245T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+178T= MANE Select	ENSP00000295897.4:n.*23+178T=
ENST00000295897.8:c.*23+178T=	ENSP00000295897.4:n.*23+178T=
ENST00000401494.7:c.*23+178T=	ENSP00000384695.3:n.*23+178T=
ENST00000415165.6:c.*23+178T=	ENSP00000401820.2:n.*23+178T=
ENST00000476441.6:c.*1132+178T=	ENSP00000423727.1:n.*1132+178T=
ENST00000495173.1:n.161+178T=
ENST00000503124.5:c.*23+178T=	ENSP00000421027.1:n.*23+178T=
ENST00000505649.5:n.1400+178T=
ENST00000508932.5:n.243+178T=
ENST00000509063.5:c.1786-593T=	ENSP00000422784.1:n.1786-593T=
ENST00000511370.1:c.1386+178T=
ENST00000621085.4:c.*23+178T=	ENSP00000483421.1:n.*23+178T=
ENST00000621628.4:c.*23+178T=	ENSP00000480485.1:n.*23+178T=
NM_000477.5:c.*23+178T=	NP_000468.1:n.*23+178T=
NM_000477.6:c.*23+178T=	NP_000468.1:n.*23+178T=
NM_000477.7:c.*23+178T= MANE Select	NP_000468.1:n.*23+178T=