Canonical Allele Identifier: CA357244484

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283889T>A (hg19) ; chr4:g.73418172T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418172T>A , CM000666.2:g.73418172T>A	GRCh38
NC_000004.11:g.74283889T>A , CM000666.1:g.74283889T>A	GRCh37
NC_000004.10:g.74502753T>A	NCBI36
NG_009291.1:g.18918T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1513T>A MANE Select	ENSP00000295897.4:p.Leu505Met
ENST00000295897.8:c.1513T>A	ENSP00000295897.4:p.Leu505Met
ENST00000401494.7:c.1168T>A	ENSP00000384695.3:p.Leu390Met
ENST00000415165.6:c.937T>A	ENSP00000401820.2:p.Leu313Met
ENST00000476441.6:c.*792T>A	ENSP00000423727.1:n.*792T>A
ENST00000486939.1:n.167T>A
ENST00000503124.5:c.1063T>A	ENSP00000421027.1:p.Leu355Met
ENST00000505649.5:n.1060T>A
ENST00000509063.5:c.1513T>A	ENSP00000422784.1:p.Leu505Met
ENST00000511370.1:c.1046T>A
ENST00000621085.4:c.874T>A	ENSP00000483421.1:p.Leu292Met
ENST00000621628.4:c.874T>A	ENSP00000480485.1:p.Leu292Met
NM_000477.5:c.1513T>A	NP_000468.1:p.Leu505Met
NM_000477.6:c.1513T>A	NP_000468.1:p.Leu505Met
NM_000477.7:c.1513T>A MANE Select	NP_000468.1:p.Leu505Met