Canonical Allele Identifier: CA1468143565

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415125G= , CM000666.2:g.73415125G=	GRCh38
NC_000004.11:g.74280842G= , CM000666.1:g.74280842G=	GRCh37
NC_000004.10:g.74499706G=	NCBI36
NG_009291.1:g.15871G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1149G= MANE Select	ENSP00000295897.4:p.Lys383=
ENST00000295897.8:c.1149G=	ENSP00000295897.4:p.Lys383=
ENST00000401494.7:c.804G=	ENSP00000384695.3:p.Lys268=
ENST00000415165.6:c.573G=	ENSP00000401820.2:p.Lys191=
ENST00000476441.6:c.*428G=	ENSP00000423727.1:n.*428G=
ENST00000484992.1:n.469G=
ENST00000503124.5:c.699G=	ENSP00000421027.1:p.Lys233=
ENST00000504043.1:n.152G=
ENST00000505649.5:n.835G=
ENST00000509063.5:c.1149G=	ENSP00000422784.1:p.Lys383=
ENST00000511370.1:c.682G=
ENST00000621085.4:c.510G=	ENSP00000483421.1:p.Lys170=
ENST00000621628.4:c.510G=	ENSP00000480485.1:p.Lys170=
NM_000477.5:c.1149G=	NP_000468.1:p.Lys383=
NM_000477.6:c.1149G=	NP_000468.1:p.Lys383=
NM_000477.7:c.1149G= MANE Select	NP_000468.1:p.Lys383=