Canonical Allele Identifier: CA357241578

Gene: ALB

Linked Data

• gnomAD v4: 4-73415157-A-G
• MyVariant Identifiers: chr4:g.74280874A>G (hg19) ; chr4:g.73415157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415157A>G , CM000666.2:g.73415157A>G	GRCh38
NC_000004.11:g.74280874A>G , CM000666.1:g.74280874A>G	GRCh37
NC_000004.10:g.74499738A>G	NCBI36
NG_009291.1:g.15903A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1181A>G MANE Select	ENSP00000295897.4:p.Tyr394Cys
ENST00000295897.8:c.1181A>G	ENSP00000295897.4:p.Tyr394Cys
ENST00000401494.7:c.836A>G	ENSP00000384695.3:p.Tyr279Cys
ENST00000415165.6:c.605A>G	ENSP00000401820.2:p.Tyr202Cys
ENST00000476441.6:c.*460A>G	ENSP00000423727.1:n.*460A>G
ENST00000484992.1:n.501A>G
ENST00000503124.5:c.731A>G	ENSP00000421027.1:p.Tyr244Cys
ENST00000504043.1:n.184A>G
ENST00000505649.5:n.867A>G
ENST00000509063.5:c.1181A>G	ENSP00000422784.1:p.Tyr394Cys
ENST00000511370.1:c.714A>G
ENST00000621085.4:c.542A>G	ENSP00000483421.1:p.Tyr181Cys
ENST00000621628.4:c.542A>G	ENSP00000480485.1:p.Tyr181Cys
NM_000477.5:c.1181A>G	NP_000468.1:p.Tyr394Cys
NM_000477.6:c.1181A>G	NP_000468.1:p.Tyr394Cys
NM_000477.7:c.1181A>G MANE Select	NP_000468.1:p.Tyr394Cys