Canonical Allele Identifier: CA357239074

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74277721C>T (hg19) ; chr4:g.73412004C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73412004C>T , CM000666.2:g.73412004C>T	GRCh38
NC_000004.11:g.74277721C>T , CM000666.1:g.74277721C>T	GRCh37
NC_000004.10:g.74496585C>T	NCBI36
NG_009291.1:g.12750C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.722C>T MANE Select	ENSP00000295897.4:p.Ala241Val
ENST00000295897.8:c.722C>T	ENSP00000295897.4:p.Ala241Val
ENST00000401494.7:c.377C>T	ENSP00000384695.3:p.Ala126Val
ENST00000415165.6:c.146C>T	ENSP00000401820.2:p.Ala49Val
ENST00000476441.6:c.*1C>T	ENSP00000423727.1:n.*1C>T
ENST00000503124.5:c.272C>T	ENSP00000421027.1:p.Ala91Val
ENST00000505649.5:n.408C>T
ENST00000507673.1:n.39C>T
ENST00000509063.5:c.722C>T	ENSP00000422784.1:p.Ala241Val
ENST00000511370.1:c.255C>T
ENST00000621085.4:c.490+2642C>T	ENSP00000483421.1:n.490+2642C>T
ENST00000621628.4:c.486+2928C>T	ENSP00000480485.1:n.486+2928C>T
NM_000477.5:c.722C>T	NP_000468.1:p.Ala241Val
NM_000477.6:c.722C>T	NP_000468.1:p.Ala241Val
NM_000477.7:c.722C>T MANE Select	NP_000468.1:p.Ala241Val