Canonical Allele Identifier: CA439800857

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285230T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419513T>G , CM000666.2:g.73419513T>G	GRCh38
NC_000004.11:g.74285230T>G , CM000666.1:g.74285230T>G	GRCh37
NC_000004.10:g.74504094T>G	NCBI36
NG_009291.1:g.20259T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1659T>G MANE Select	ENSP00000295897.4:p.Leu553=
ENST00000295897.8:c.1659T>G	ENSP00000295897.4:p.Leu553=
ENST00000401494.7:c.1314T>G	ENSP00000384695.3:p.Leu438=
ENST00000415165.6:c.1083T>G	ENSP00000401820.2:p.Leu361=
ENST00000476441.6:c.*938T>G	ENSP00000423727.1:n.*938T>G
ENST00000486939.1:n.313T>G
ENST00000503124.5:c.1209T>G	ENSP00000421027.1:p.Leu403=
ENST00000505649.5:n.1206T>G
ENST00000508932.5:n.175+58T>G
ENST00000509063.5:c.1659T>G	ENSP00000422784.1:p.Leu553=
ENST00000511370.1:c.1192T>G
ENST00000621085.4:c.1020T>G	ENSP00000483421.1:p.Leu340=
ENST00000621628.4:c.1020T>G	ENSP00000480485.1:p.Leu340=
NM_000477.5:c.1659T>G	NP_000468.1:p.Leu553=
NM_000477.6:c.1659T>G	NP_000468.1:p.Leu553=
NM_000477.7:c.1659T>G MANE Select	NP_000468.1:p.Leu553=