Canonical Allele Identifier: CA357246151

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285255A>G (hg19) ; chr4:g.73419538A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419538A>G , CM000666.2:g.73419538A>G	GRCh38
NC_000004.11:g.74285255A>G , CM000666.1:g.74285255A>G	GRCh37
NC_000004.10:g.74504119A>G	NCBI36
NG_009291.1:g.20284A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1684A>G MANE Select	ENSP00000295897.4:p.Lys562Glu
ENST00000295897.8:c.1684A>G	ENSP00000295897.4:p.Lys562Glu
ENST00000401494.7:c.1339A>G	ENSP00000384695.3:p.Lys447Glu
ENST00000415165.6:c.1108A>G	ENSP00000401820.2:p.Lys370Glu
ENST00000476441.6:c.*963A>G	ENSP00000423727.1:n.*963A>G
ENST00000486939.1:n.338A>G
ENST00000503124.5:c.1234A>G	ENSP00000421027.1:p.Lys412Glu
ENST00000505649.5:n.1231A>G
ENST00000508932.5:n.175+83A>G
ENST00000509063.5:c.1684A>G	ENSP00000422784.1:p.Lys562Glu
ENST00000511370.1:c.1217A>G
ENST00000621085.4:c.1045A>G	ENSP00000483421.1:p.Lys349Glu
ENST00000621628.4:c.1045A>G	ENSP00000480485.1:p.Lys349Glu
NM_000477.5:c.1684A>G	NP_000468.1:p.Lys562Glu
NM_000477.6:c.1684A>G	NP_000468.1:p.Lys562Glu
NM_000477.7:c.1684A>G MANE Select	NP_000468.1:p.Lys562Glu