Canonical Allele Identifier: CA1468146793

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418131C= , CM000666.2:g.73418131C=	GRCh38
NC_000004.11:g.74283848C= , CM000666.1:g.74283848C=	GRCh37
NC_000004.10:g.74502712C=	NCBI36
NG_009291.1:g.18877C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1472C= MANE Select	ENSP00000295897.4:p.Thr491=
ENST00000295897.8:c.1472C=	ENSP00000295897.4:p.Thr491=
ENST00000401494.7:c.1127C=	ENSP00000384695.3:p.Thr376=
ENST00000415165.6:c.896C=	ENSP00000401820.2:p.Thr299=
ENST00000476441.6:c.*751C=	ENSP00000423727.1:n.*751C=
ENST00000486939.1:n.126C=
ENST00000503124.5:c.1022C=	ENSP00000421027.1:p.Thr341=
ENST00000505649.5:n.1019C=
ENST00000509063.5:c.1472C=	ENSP00000422784.1:p.Thr491=
ENST00000511370.1:c.1005C=
ENST00000621085.4:c.833C=	ENSP00000483421.1:p.Thr278=
ENST00000621628.4:c.833C=	ENSP00000480485.1:p.Thr278=
NM_000477.5:c.1472C=	NP_000468.1:p.Thr491=
NM_000477.6:c.1472C=	NP_000468.1:p.Thr491=
NM_000477.7:c.1472C= MANE Select	NP_000468.1:p.Thr491=