Canonical Allele Identifier: CA1468150872

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406657C= , CM000666.2:g.73406657C=	GRCh38
NC_000004.11:g.74272374C= , CM000666.1:g.74272374C=	GRCh37
NC_000004.10:g.74491238C=	NCBI36
NG_009291.1:g.7403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.166C= MANE Select	ENSP00000295897.4:p.Gln56=
ENST00000295897.8:c.166C=	ENSP00000295897.4:p.Gln56=
ENST00000401494.7:c.137+1484C=	ENSP00000384695.3:n.137+1484C=
ENST00000415165.6:c.137+1484C=	ENSP00000401820.2:n.137+1484C=
ENST00000441319.5:c.172C=	ENSP00000392541.1:p.Gln58=
ENST00000476441.6:c.79+2251C=	ENSP00000423727.1:n.79+2251C=
ENST00000503124.5:c.-73C=	ENSP00000421027.1:n.-73C=
ENST00000509063.5:c.166C=	ENSP00000422784.1:p.Gln56=
ENST00000510166.5:n.202C=
ENST00000514786.1:n.135C=
ENST00000515133.5:n.207C=
ENST00000621085.4:c.166C=	ENSP00000483421.1:p.Gln56=
ENST00000621628.4:c.166C=	ENSP00000480485.1:p.Gln56=
NM_000477.5:c.166C=	NP_000468.1:p.Gln56=
NM_000477.6:c.166C=	NP_000468.1:p.Gln56=
NM_000477.7:c.166C= MANE Select	NP_000468.1:p.Gln56=