Canonical Allele Identifier: CA357240530

Gene: ALB

Linked Data

• gnomAD v4: 4-73413456-T-G
• MyVariant Identifiers: chr4:g.74279173T>G (hg19) ; chr4:g.73413456T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413456T>G , CM000666.2:g.73413456T>G	GRCh38
NC_000004.11:g.74279173T>G , CM000666.1:g.74279173T>G	GRCh37
NC_000004.10:g.74498037T>G	NCBI36
NG_009291.1:g.14202T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.880T>G MANE Select	ENSP00000295897.4:p.Ser294Ala
ENST00000295897.8:c.880T>G	ENSP00000295897.4:p.Ser294Ala
ENST00000401494.7:c.535T>G	ENSP00000384695.3:p.Ser179Ala
ENST00000415165.6:c.304T>G	ENSP00000401820.2:p.Ser102Ala
ENST00000476441.6:c.*159T>G	ENSP00000423727.1:n.*159T>G
ENST00000484992.1:n.200T>G
ENST00000503124.5:c.430T>G	ENSP00000421027.1:p.Ser144Ala
ENST00000505649.5:n.566T>G
ENST00000509063.5:c.880T>G	ENSP00000422784.1:p.Ser294Ala
ENST00000511370.1:c.413T>G
ENST00000621085.4:c.491-1650T>G	ENSP00000483421.1:n.491-1650T>G
ENST00000621628.4:c.487-1646T>G	ENSP00000480485.1:n.487-1646T>G
NM_000477.5:c.880T>G	NP_000468.1:p.Ser294Ala
NM_000477.6:c.880T>G	NP_000468.1:p.Ser294Ala
NM_000477.7:c.880T>G MANE Select	NP_000468.1:p.Ser294Ala