Canonical Allele Identifier: CA1468148550

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419875C= , CM000666.2:g.73419875C=	GRCh38
NC_000004.11:g.74285592C= , CM000666.1:g.74285592C=	GRCh37
NC_000004.10:g.74504456C=	NCBI36
NG_009291.1:g.20621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+236C= MANE Select	ENSP00000295897.4:n.1785+236C=
ENST00000295897.8:c.1785+236C=	ENSP00000295897.4:n.1785+236C=
ENST00000401494.7:c.1440+236C=	ENSP00000384695.3:n.1440+236C=
ENST00000415165.6:c.1209+236C=	ENSP00000401820.2:n.1209+236C=
ENST00000476441.6:c.*1064+236C=	ENSP00000423727.1:n.*1064+236C=
ENST00000495173.1:n.93+236C=
ENST00000503124.5:c.1335+236C=	ENSP00000421027.1:n.1335+236C=
ENST00000505649.5:n.1332+236C=
ENST00000508932.5:n.176-379C=
ENST00000509063.5:c.1785+236C=	ENSP00000422784.1:n.1785+236C=
ENST00000511370.1:c.1318+236C=
ENST00000621085.4:c.1146+236C=	ENSP00000483421.1:n.1146+236C=
ENST00000621628.4:c.1146+236C=	ENSP00000480485.1:n.1146+236C=
NM_000477.5:c.1785+236C=	NP_000468.1:n.1785+236C=
NM_000477.6:c.1785+236C=	NP_000468.1:n.1785+236C=
NM_000477.7:c.1785+236C= MANE Select	NP_000468.1:n.1785+236C=