Canonical Allele Identifier: CA1468146698

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418085T= , CM000666.2:g.73418085T=	GRCh38
NC_000004.11:g.74283802T= , CM000666.1:g.74283802T=	GRCh37
NC_000004.10:g.74502666T=	NCBI36
NG_009291.1:g.18831T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1429-3T= MANE Select	ENSP00000295897.4:n.1429-3T=
ENST00000295897.8:c.1429-3T=	ENSP00000295897.4:n.1429-3T=
ENST00000401494.7:c.1084-3T=	ENSP00000384695.3:n.1084-3T=
ENST00000415165.6:c.853-3T=	ENSP00000401820.2:n.853-3T=
ENST00000476441.6:c.*708-3T=	ENSP00000423727.1:n.*708-3T=
ENST00000486939.1:n.80T=
ENST00000503124.5:c.979-3T=	ENSP00000421027.1:n.979-3T=
ENST00000505649.5:n.976-3T=
ENST00000509063.5:c.1429-3T=	ENSP00000422784.1:n.1429-3T=
ENST00000511370.1:c.962-3T=
ENST00000621085.4:c.790-3T=	ENSP00000483421.1:n.790-3T=
ENST00000621628.4:c.790-3T=	ENSP00000480485.1:n.790-3T=
NM_000477.5:c.1429-3T=	NP_000468.1:n.1429-3T=
NM_000477.6:c.1429-3T=	NP_000468.1:n.1429-3T=
NM_000477.7:c.1429-3T= MANE Select	NP_000468.1:n.1429-3T=