Canonical Allele Identifier: CA1468143669

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415168G= , CM000666.2:g.73415168G=	GRCh38
NC_000004.11:g.74280885G= , CM000666.1:g.74280885G=	GRCh37
NC_000004.10:g.74499749G=	NCBI36
NG_009291.1:g.15914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+1G= MANE Select	ENSP00000295897.4:n.1191+1G=
ENST00000295897.8:c.1191+1G=	ENSP00000295897.4:n.1191+1G=
ENST00000401494.7:c.846+1G=	ENSP00000384695.3:n.846+1G=
ENST00000415165.6:c.615+1G=	ENSP00000401820.2:n.615+1G=
ENST00000476441.6:c.*470+1G=	ENSP00000423727.1:n.*470+1G=
ENST00000484992.1:n.511+1G=
ENST00000503124.5:c.741+1G=	ENSP00000421027.1:n.741+1G=
ENST00000504043.1:n.195G=
ENST00000505649.5:n.877+1G=
ENST00000509063.5:c.1191+1G=	ENSP00000422784.1:n.1191+1G=
ENST00000511370.1:c.724+1G=
ENST00000621085.4:c.552+1G=	ENSP00000483421.1:n.552+1G=
ENST00000621628.4:c.552+1G=	ENSP00000480485.1:n.552+1G=
NM_000477.5:c.1191+1G=	NP_000468.1:n.1191+1G=
NM_000477.6:c.1191+1G=	NP_000468.1:n.1191+1G=
NM_000477.7:c.1191+1G= MANE Select	NP_000468.1:n.1191+1G=