Canonical Allele Identifier: CA1468143431

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415055G= , CM000666.2:g.73415055G=	GRCh38
NC_000004.11:g.74280772G= , CM000666.1:g.74280772G=	GRCh37
NC_000004.10:g.74499636G=	NCBI36
NG_009291.1:g.15801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1079G= MANE Select	ENSP00000295897.4:p.Arg360=
ENST00000295897.8:c.1079G=	ENSP00000295897.4:p.Arg360=
ENST00000401494.7:c.734G=	ENSP00000384695.3:p.Arg245=
ENST00000415165.6:c.503G=	ENSP00000401820.2:p.Arg168=
ENST00000476441.6:c.*358G=	ENSP00000423727.1:n.*358G=
ENST00000484992.1:n.399G=
ENST00000503124.5:c.629G=	ENSP00000421027.1:p.Arg210=
ENST00000504043.1:n.82G=
ENST00000505649.5:n.765G=
ENST00000509063.5:c.1079G=	ENSP00000422784.1:p.Arg360=
ENST00000511370.1:c.612G=
ENST00000621085.4:c.491-51G=	ENSP00000483421.1:n.491-51G=
ENST00000621628.4:c.487-47G=	ENSP00000480485.1:n.487-47G=
NM_000477.5:c.1079G=	NP_000468.1:p.Arg360=
NM_000477.6:c.1079G=	NP_000468.1:p.Arg360=
NM_000477.7:c.1079G= MANE Select	NP_000468.1:p.Arg360=