Canonical Allele Identifier: CA1468143605

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415141G= , CM000666.2:g.73415141G=	GRCh38
NC_000004.11:g.74280858G= , CM000666.1:g.74280858G=	GRCh37
NC_000004.10:g.74499722G=	NCBI36
NG_009291.1:g.15887G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1165G= MANE Select	NP_000468.1:p.Asp389=
ENST00000295897.9:c.1165G= MANE Select	ENSP00000295897.4:p.Asp389=
NM_000477.5:c.1165G=	NP_000468.1:p.Asp389=
NM_000477.6:c.1165G=	NP_000468.1:p.Asp389=
ENST00000295897.8:c.1165G=	ENSP00000295897.4:p.Asp389=
ENST00000401494.7:c.820G=	ENSP00000384695.3:p.Asp274=
ENST00000415165.6:c.589G=	ENSP00000401820.2:p.Asp197=
ENST00000476441.6:c.*444G=	ENSP00000423727.1:n.*444G=
ENST00000484992.1:n.485G=
ENST00000503124.5:c.715G=	ENSP00000421027.1:p.Asp239=
ENST00000504043.1:n.168G=
ENST00000505649.5:n.851G=
ENST00000509063.5:c.1165G=	ENSP00000422784.1:p.Asp389=
ENST00000511370.1:c.698G=
ENST00000621085.4:c.526G=	ENSP00000483421.1:p.Asp176=
ENST00000621628.4:c.526G=	ENSP00000480485.1:p.Asp176=