Canonical Allele Identifier: CA357238376

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275196T>A (hg19) ; chr4:g.73409479T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409479T>A , CM000666.2:g.73409479T>A	GRCh38
NC_000004.11:g.74275196T>A , CM000666.1:g.74275196T>A	GRCh37
NC_000004.10:g.74494060T>A	NCBI36
NG_009291.1:g.10225T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.607T>A MANE Select	ENSP00000295897.4:p.Leu203Met
ENST00000295897.8:c.607T>A	ENSP00000295897.4:p.Leu203Met
ENST00000401494.7:c.262T>A	ENSP00000384695.3:p.Leu88Met
ENST00000415165.6:c.138-2517T>A	ENSP00000401820.2:n.138-2517T>A
ENST00000476441.6:c.204T>A	ENSP00000423727.1:p.Cys68Ter
ENST00000503124.5:c.157T>A	ENSP00000421027.1:p.Leu53Met
ENST00000505649.5:n.293T>A
ENST00000509063.5:c.607T>A	ENSP00000422784.1:p.Leu203Met
ENST00000511370.1:c.140T>A
ENST00000514786.1:n.576T>A
ENST00000621085.4:c.490+117T>A	ENSP00000483421.1:n.490+117T>A
ENST00000621628.4:c.486+403T>A	ENSP00000480485.1:n.486+403T>A
NM_000477.5:c.607T>A	NP_000468.1:p.Leu203Met
NM_000477.6:c.607T>A	NP_000468.1:p.Leu203Met
NM_000477.7:c.607T>A MANE Select	NP_000468.1:p.Leu203Met