Canonical Allele Identifier: CA1468148577

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419930C= , CM000666.2:g.73419930C=	GRCh38
NC_000004.11:g.74285647C= , CM000666.1:g.74285647C=	GRCh37
NC_000004.10:g.74504511C=	NCBI36
NG_009291.1:g.20676C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+291C= MANE Select	ENSP00000295897.4:n.1785+291C=
ENST00000295897.8:c.1785+291C=	ENSP00000295897.4:n.1785+291C=
ENST00000401494.7:c.1440+291C=	ENSP00000384695.3:n.1440+291C=
ENST00000415165.6:c.1209+291C=	ENSP00000401820.2:n.1209+291C=
ENST00000476441.6:c.*1064+291C=	ENSP00000423727.1:n.*1064+291C=
ENST00000495173.1:n.93+291C=
ENST00000503124.5:c.1335+291C=	ENSP00000421027.1:n.1335+291C=
ENST00000505649.5:n.1332+291C=
ENST00000508932.5:n.176-324C=
ENST00000509063.5:c.1785+291C=	ENSP00000422784.1:n.1785+291C=
ENST00000511370.1:c.1318+291C=
ENST00000621085.4:c.1146+291C=	ENSP00000483421.1:n.1146+291C=
ENST00000621628.4:c.1146+291C=	ENSP00000480485.1:n.1146+291C=
NM_000477.5:c.1785+291C=	NP_000468.1:n.1785+291C=
NM_000477.6:c.1785+291C=	NP_000468.1:n.1785+291C=
NM_000477.7:c.1785+291C= MANE Select	NP_000468.1:n.1785+291C=