Canonical Allele Identifier: CA357241517

Gene: ALB

Linked Data

• gnomAD v4: 4-73415149-T-A
• MyVariant Identifiers: chr4:g.74280866T>A (hg19) ; chr4:g.73415149T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415149T>A , CM000666.2:g.73415149T>A	GRCh38
NC_000004.11:g.74280866T>A , CM000666.1:g.74280866T>A	GRCh37
NC_000004.10:g.74499730T>A	NCBI36
NG_009291.1:g.15895T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1173T>A MANE Select	ENSP00000295897.4:p.His391Gln
ENST00000295897.8:c.1173T>A	ENSP00000295897.4:p.His391Gln
ENST00000401494.7:c.828T>A	ENSP00000384695.3:p.His276Gln
ENST00000415165.6:c.597T>A	ENSP00000401820.2:p.His199Gln
ENST00000476441.6:c.*452T>A	ENSP00000423727.1:n.*452T>A
ENST00000484992.1:n.493T>A
ENST00000503124.5:c.723T>A	ENSP00000421027.1:p.His241Gln
ENST00000504043.1:n.176T>A
ENST00000505649.5:n.859T>A
ENST00000509063.5:c.1173T>A	ENSP00000422784.1:p.His391Gln
ENST00000511370.1:c.706T>A
ENST00000621085.4:c.534T>A	ENSP00000483421.1:p.His178Gln
ENST00000621628.4:c.534T>A	ENSP00000480485.1:p.His178Gln
NM_000477.5:c.1173T>A	NP_000468.1:p.His391Gln
NM_000477.6:c.1173T>A	NP_000468.1:p.His391Gln
NM_000477.7:c.1173T>A MANE Select	NP_000468.1:p.His391Gln