Canonical Allele Identifier: CA1468143699

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415180T= , CM000666.2:g.73415180T=	GRCh38
NC_000004.11:g.74280897T= , CM000666.1:g.74280897T=	GRCh37
NC_000004.10:g.74499761T=	NCBI36
NG_009291.1:g.15926T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1191+13T= MANE Select	ENSP00000295897.4:n.1191+13T=
ENST00000295897.8:c.1191+13T=	ENSP00000295897.4:n.1191+13T=
ENST00000401494.7:c.846+13T=	ENSP00000384695.3:n.846+13T=
ENST00000415165.6:c.615+13T=	ENSP00000401820.2:n.615+13T=
ENST00000476441.6:c.*470+13T=	ENSP00000423727.1:n.*470+13T=
ENST00000484992.1:n.511+13T=
ENST00000503124.5:c.741+13T=	ENSP00000421027.1:n.741+13T=
ENST00000504043.1:n.207T=
ENST00000505649.5:n.877+13T=
ENST00000509063.5:c.1191+13T=	ENSP00000422784.1:n.1191+13T=
ENST00000511370.1:c.724+13T=
ENST00000621085.4:c.552+13T=	ENSP00000483421.1:n.552+13T=
ENST00000621628.4:c.552+13T=	ENSP00000480485.1:n.552+13T=
NM_000477.5:c.1191+13T=	NP_000468.1:n.1191+13T=
NM_000477.6:c.1191+13T=	NP_000468.1:n.1191+13T=
NM_000477.7:c.1191+13T= MANE Select	NP_000468.1:n.1191+13T=