Canonical Allele Identifier: CA357247180

Gene: ALB

Linked Data

• dbSNP Id: rs1293883614
• gnomAD v4: 4-73420276-G-A
• MyVariant Identifiers: chr4:g.74285993G>A (hg19) ; chr4:g.73420276G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420276G>A , CM000666.2:g.73420276G>A	GRCh38
NC_000004.11:g.74285993G>A , CM000666.1:g.74285993G>A	GRCh37
NC_000004.10:g.74504857G>A	NCBI36
NG_009291.1:g.21022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1808G>A MANE Select	ENSP00000295897.4:p.Ser603Asn
ENST00000295897.8:c.1808G>A	ENSP00000295897.4:p.Ser603Asn
ENST00000401494.7:c.1463G>A	ENSP00000384695.3:p.Ser488Asn
ENST00000415165.6:c.1232G>A	ENSP00000401820.2:p.Ser411Asn
ENST00000476441.6:c.*1087G>A	ENSP00000423727.1:n.*1087G>A
ENST00000495173.1:n.116G>A
ENST00000503124.5:c.1358G>A	ENSP00000421027.1:p.Ser453Asn
ENST00000505649.5:n.1355G>A
ENST00000508932.5:n.198G>A
ENST00000509063.5:c.1785+637G>A	ENSP00000422784.1:n.1785+637G>A
ENST00000511370.1:c.1341G>A
ENST00000621085.4:c.1169G>A	ENSP00000483421.1:p.Ser390Asn
ENST00000621628.4:c.1169G>A	ENSP00000480485.1:p.Ser390Asn
NM_000477.5:c.1808G>A	NP_000468.1:p.Ser603Asn
NM_000477.6:c.1808G>A	NP_000468.1:p.Ser603Asn
NM_000477.7:c.1808G>A MANE Select	NP_000468.1:p.Ser603Asn