Canonical Allele Identifier: CA439800327

Gene: ALB

Linked Data

• gnomAD v4: 4-73415116-T-A
• MyVariant Identifiers: chr4:g.74280833T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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