Canonical Allele Identifier: CA439800329

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280833T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415116T>G , CM000666.2:g.73415116T>G	GRCh38
NC_000004.11:g.74280833T>G , CM000666.1:g.74280833T>G	GRCh37
NC_000004.10:g.74499697T>G	NCBI36
NG_009291.1:g.15862T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1140T>G MANE Select	ENSP00000295897.4:p.Thr380=
ENST00000295897.8:c.1140T>G	ENSP00000295897.4:p.Thr380=
ENST00000401494.7:c.795T>G	ENSP00000384695.3:p.Thr265=
ENST00000415165.6:c.564T>G	ENSP00000401820.2:p.Thr188=
ENST00000476441.6:c.*419T>G	ENSP00000423727.1:n.*419T>G
ENST00000484992.1:n.460T>G
ENST00000503124.5:c.690T>G	ENSP00000421027.1:p.Thr230=
ENST00000504043.1:n.143T>G
ENST00000505649.5:n.826T>G
ENST00000509063.5:c.1140T>G	ENSP00000422784.1:p.Thr380=
ENST00000511370.1:c.673T>G
ENST00000621085.4:c.501T>G	ENSP00000483421.1:p.Thr167=
ENST00000621628.4:c.501T>G	ENSP00000480485.1:p.Thr167=
NM_000477.5:c.1140T>G	NP_000468.1:p.Thr380=
NM_000477.6:c.1140T>G	NP_000468.1:p.Thr380=
NM_000477.7:c.1140T>G MANE Select	NP_000468.1:p.Thr380=