Canonical Allele Identifier: CA357236059

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272462A>T (hg19) ; chr4:g.73406745A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406745A>T , CM000666.2:g.73406745A>T	GRCh38
NC_000004.11:g.74272462A>T , CM000666.1:g.74272462A>T	GRCh37
NC_000004.10:g.74491326A>T	NCBI36
NG_009291.1:g.7491A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.254A>T MANE Select	ENSP00000295897.4:p.Asn85Ile
ENST00000295897.8:c.254A>T	ENSP00000295897.4:p.Asn85Ile
ENST00000401494.7:c.137+1572A>T	ENSP00000384695.3:n.137+1572A>T
ENST00000415165.6:c.137+1572A>T	ENSP00000401820.2:n.137+1572A>T
ENST00000441319.5:c.260A>T	ENSP00000392541.1:p.Asn87Ile
ENST00000476441.6:c.79+2339A>T	ENSP00000423727.1:n.79+2339A>T
ENST00000503124.5:c.16A>T	ENSP00000421027.1:p.Ile6Phe
ENST00000509063.5:c.254A>T	ENSP00000422784.1:p.Asn85Ile
ENST00000510166.5:n.290A>T
ENST00000514786.1:n.223A>T
ENST00000515133.5:n.295A>T
ENST00000621085.4:c.254A>T	ENSP00000483421.1:p.Asn85Ile
ENST00000621628.4:c.254A>T	ENSP00000480485.1:p.Asn85Ile
NM_000477.5:c.254A>T	NP_000468.1:p.Asn85Ile
NM_000477.6:c.254A>T	NP_000468.1:p.Asn85Ile
NM_000477.7:c.254A>T MANE Select	NP_000468.1:p.Asn85Ile