Canonical Allele Identifier: CA357244321

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283860A>T (hg19) ; chr4:g.73418143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418143A>T , CM000666.2:g.73418143A>T	GRCh38
NC_000004.11:g.74283860A>T , CM000666.1:g.74283860A>T	GRCh37
NC_000004.10:g.74502724A>T	NCBI36
NG_009291.1:g.18889A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1484A>T MANE Select	ENSP00000295897.4:p.Asp495Val
ENST00000295897.8:c.1484A>T	ENSP00000295897.4:p.Asp495Val
ENST00000401494.7:c.1139A>T	ENSP00000384695.3:p.Asp380Val
ENST00000415165.6:c.908A>T	ENSP00000401820.2:p.Asp303Val
ENST00000476441.6:c.*763A>T	ENSP00000423727.1:n.*763A>T
ENST00000486939.1:n.138A>T
ENST00000503124.5:c.1034A>T	ENSP00000421027.1:p.Asp345Val
ENST00000505649.5:n.1031A>T
ENST00000509063.5:c.1484A>T	ENSP00000422784.1:p.Asp495Val
ENST00000511370.1:c.1017A>T
ENST00000621085.4:c.845A>T	ENSP00000483421.1:p.Asp282Val
ENST00000621628.4:c.845A>T	ENSP00000480485.1:p.Asp282Val
NM_000477.5:c.1484A>T	NP_000468.1:p.Asp495Val
NM_000477.6:c.1484A>T	NP_000468.1:p.Asp495Val
NM_000477.7:c.1484A>T MANE Select	NP_000468.1:p.Asp495Val