Canonical Allele Identifier: CA439948345

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283861C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418144C>T , CM000666.2:g.73418144C>T	GRCh38
NC_000004.11:g.74283861C>T , CM000666.1:g.74283861C>T	GRCh37
NC_000004.10:g.74502725C>T	NCBI36
NG_009291.1:g.18890C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1485C>T MANE Select	ENSP00000295897.4:p.Asp495=
ENST00000295897.8:c.1485C>T	ENSP00000295897.4:p.Asp495=
ENST00000401494.7:c.1140C>T	ENSP00000384695.3:p.Asp380=
ENST00000415165.6:c.909C>T	ENSP00000401820.2:p.Asp303=
ENST00000476441.6:c.*764C>T	ENSP00000423727.1:n.*764C>T
ENST00000486939.1:n.139C>T
ENST00000503124.5:c.1035C>T	ENSP00000421027.1:p.Asp345=
ENST00000505649.5:n.1032C>T
ENST00000509063.5:c.1485C>T	ENSP00000422784.1:p.Asp495=
ENST00000511370.1:c.1018C>T
ENST00000621085.4:c.846C>T	ENSP00000483421.1:p.Asp282=
ENST00000621628.4:c.846C>T	ENSP00000480485.1:p.Asp282=
NM_000477.5:c.1485C>T	NP_000468.1:p.Asp495=
NM_000477.6:c.1485C>T	NP_000468.1:p.Asp495=
NM_000477.7:c.1485C>T MANE Select	NP_000468.1:p.Asp495=