Canonical Allele Identifier: CA357247253

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286005T>A (hg19) ; chr4:g.73420288T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420288T>A , CM000666.2:g.73420288T>A	GRCh38
NC_000004.11:g.74286005T>A , CM000666.1:g.74286005T>A	GRCh37
NC_000004.10:g.74504869T>A	NCBI36
NG_009291.1:g.21034T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1820T>A MANE Select	ENSP00000295897.4:p.Leu607Ter
ENST00000295897.8:c.1820T>A	ENSP00000295897.4:p.Leu607Ter
ENST00000401494.7:c.1475T>A	ENSP00000384695.3:p.Leu492Ter
ENST00000415165.6:c.1244T>A	ENSP00000401820.2:p.Leu415Ter
ENST00000476441.6:c.*1099T>A	ENSP00000423727.1:n.*1099T>A
ENST00000495173.1:n.128T>A
ENST00000503124.5:c.1370T>A	ENSP00000421027.1:p.Leu457Ter
ENST00000505649.5:n.1367T>A
ENST00000508932.5:n.210T>A
ENST00000509063.5:c.1785+649T>A	ENSP00000422784.1:n.1785+649T>A
ENST00000511370.1:c.1353T>A
ENST00000621085.4:c.1181T>A	ENSP00000483421.1:p.Leu394Ter
ENST00000621628.4:c.1181T>A	ENSP00000480485.1:p.Leu394Ter
NM_000477.5:c.1820T>A	NP_000468.1:p.Leu607Ter
NM_000477.6:c.1820T>A	NP_000468.1:p.Leu607Ter
NM_000477.7:c.1820T>A MANE Select	NP_000468.1:p.Leu607Ter