Canonical Allele Identifier: CA357241373

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280843T>A (hg19) ; chr4:g.73415126T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415126T>A , CM000666.2:g.73415126T>A	GRCh38
NC_000004.11:g.74280843T>A , CM000666.1:g.74280843T>A	GRCh37
NC_000004.10:g.74499707T>A	NCBI36
NG_009291.1:g.15872T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1150T>A MANE Select	ENSP00000295897.4:p.Cys384Ser
ENST00000295897.8:c.1150T>A	ENSP00000295897.4:p.Cys384Ser
ENST00000401494.7:c.805T>A	ENSP00000384695.3:p.Cys269Ser
ENST00000415165.6:c.574T>A	ENSP00000401820.2:p.Cys192Ser
ENST00000476441.6:c.*429T>A	ENSP00000423727.1:n.*429T>A
ENST00000484992.1:n.470T>A
ENST00000503124.5:c.700T>A	ENSP00000421027.1:p.Cys234Ser
ENST00000504043.1:n.153T>A
ENST00000505649.5:n.836T>A
ENST00000509063.5:c.1150T>A	ENSP00000422784.1:p.Cys384Ser
ENST00000511370.1:c.683T>A
ENST00000621085.4:c.511T>A	ENSP00000483421.1:p.Cys171Ser
ENST00000621628.4:c.511T>A	ENSP00000480485.1:p.Cys171Ser
NM_000477.5:c.1150T>A	NP_000468.1:p.Cys384Ser
NM_000477.6:c.1150T>A	NP_000468.1:p.Cys384Ser
NM_000477.7:c.1150T>A MANE Select	NP_000468.1:p.Cys384Ser