Canonical Allele Identifier: CA357246269

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285277A>T (hg19) ; chr4:g.73419560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419560A>T , CM000666.2:g.73419560A>T	GRCh38
NC_000004.11:g.74285277A>T , CM000666.1:g.74285277A>T	GRCh37
NC_000004.10:g.74504141A>T	NCBI36
NG_009291.1:g.20306A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1706A>T MANE Select	ENSP00000295897.4:p.Lys569Ile
ENST00000295897.8:c.1706A>T	ENSP00000295897.4:p.Lys569Ile
ENST00000401494.7:c.1361A>T	ENSP00000384695.3:p.Lys454Ile
ENST00000415165.6:c.1130A>T	ENSP00000401820.2:p.Lys377Ile
ENST00000476441.6:c.*985A>T	ENSP00000423727.1:n.*985A>T
ENST00000495173.1:n.14A>T
ENST00000503124.5:c.1256A>T	ENSP00000421027.1:p.Lys419Ile
ENST00000505649.5:n.1253A>T
ENST00000508932.5:n.175+105A>T
ENST00000509063.5:c.1706A>T	ENSP00000422784.1:p.Lys569Ile
ENST00000511370.1:c.1239A>T
ENST00000621085.4:c.1067A>T	ENSP00000483421.1:p.Lys356Ile
ENST00000621628.4:c.1067A>T	ENSP00000480485.1:p.Lys356Ile
NM_000477.5:c.1706A>T	NP_000468.1:p.Lys569Ile
NM_000477.6:c.1706A>T	NP_000468.1:p.Lys569Ile
NM_000477.7:c.1706A>T MANE Select	NP_000468.1:p.Lys569Ile