Canonical Allele Identifier: CA357244755

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283932A>C (hg19) ; chr4:g.73418215A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418215A>C , CM000666.2:g.73418215A>C	GRCh38
NC_000004.11:g.74283932A>C , CM000666.1:g.74283932A>C	GRCh37
NC_000004.10:g.74502796A>C	NCBI36
NG_009291.1:g.18961A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1556A>C MANE Select	ENSP00000295897.4:p.Glu519Ala
ENST00000295897.8:c.1556A>C	ENSP00000295897.4:p.Glu519Ala
ENST00000401494.7:c.1211A>C	ENSP00000384695.3:p.Glu404Ala
ENST00000415165.6:c.980A>C	ENSP00000401820.2:p.Glu327Ala
ENST00000476441.6:c.*835A>C	ENSP00000423727.1:n.*835A>C
ENST00000486939.1:n.210A>C
ENST00000503124.5:c.1106A>C	ENSP00000421027.1:p.Glu369Ala
ENST00000505649.5:n.1103A>C
ENST00000509063.5:c.1556A>C	ENSP00000422784.1:p.Glu519Ala
ENST00000511370.1:c.1089A>C
ENST00000621085.4:c.917A>C	ENSP00000483421.1:p.Glu306Ala
ENST00000621628.4:c.917A>C	ENSP00000480485.1:p.Glu306Ala
NM_000477.5:c.1556A>C	NP_000468.1:p.Glu519Ala
NM_000477.6:c.1556A>C	NP_000468.1:p.Glu519Ala
NM_000477.7:c.1556A>C MANE Select	NP_000468.1:p.Glu519Ala