Canonical Allele Identifier: CA1468152707

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409440A= , CM000666.2:g.73409440A=	GRCh38
NC_000004.11:g.74275157A= , CM000666.1:g.74275157A=	GRCh37
NC_000004.10:g.74494021A=	NCBI36
NG_009291.1:g.10186A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.568A= MANE Select	ENSP00000295897.4:p.Thr190=
ENST00000295897.8:c.568A=	ENSP00000295897.4:p.Thr190=
ENST00000401494.7:c.223A=	ENSP00000384695.3:p.Thr75=
ENST00000415165.6:c.138-2556A=	ENSP00000401820.2:n.138-2556A=
ENST00000441319.5:c.574A=	ENSP00000392541.1:p.Thr192=
ENST00000476441.6:c.165A=	ENSP00000423727.1:p.Leu55=
ENST00000503124.5:c.118A=	ENSP00000421027.1:p.Thr40=
ENST00000505649.5:n.254A=
ENST00000509063.5:c.568A=	ENSP00000422784.1:p.Thr190=
ENST00000511370.1:c.101A=
ENST00000514786.1:n.537A=
ENST00000621085.4:c.490+78A=	ENSP00000483421.1:n.490+78A=
ENST00000621628.4:c.486+364A=	ENSP00000480485.1:n.486+364A=
NM_000477.5:c.568A=	NP_000468.1:p.Thr190=
NM_000477.6:c.568A=	NP_000468.1:p.Thr190=
NM_000477.7:c.568A= MANE Select	NP_000468.1:p.Thr190=