Canonical Allele Identifier: CA357237527

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274507A>T (hg19) ; chr4:g.73408790A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408790A>T , CM000666.2:g.73408790A>T	GRCh38
NC_000004.11:g.74274507A>T , CM000666.1:g.74274507A>T	GRCh37
NC_000004.10:g.74493371A>T	NCBI36
NG_009291.1:g.9536A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.467A>T MANE Select	ENSP00000295897.4:p.Glu156Val
ENST00000295897.8:c.467A>T	ENSP00000295897.4:p.Glu156Val
ENST00000401494.7:c.138-565A>T	ENSP00000384695.3:n.138-565A>T
ENST00000415165.6:c.138-3206A>T	ENSP00000401820.2:n.138-3206A>T
ENST00000441319.5:c.473A>T	ENSP00000392541.1:p.Glu158Val
ENST00000476441.6:c.80-565A>T	ENSP00000423727.1:n.80-565A>T
ENST00000503124.5:c.33-565A>T	ENSP00000421027.1:n.33-565A>T
ENST00000505649.5:n.153A>T
ENST00000509063.5:c.467A>T	ENSP00000422784.1:p.Glu156Val
ENST00000510166.5:n.503A>T
ENST00000514786.1:n.436A>T
ENST00000515133.5:n.508A>T
ENST00000621085.4:c.467A>T	ENSP00000483421.1:p.Glu156Val
ENST00000621628.4:c.467A>T	ENSP00000480485.1:p.Glu156Val
NM_000477.5:c.467A>T	NP_000468.1:p.Glu156Val
NM_000477.6:c.467A>T	NP_000468.1:p.Glu156Val
NM_000477.7:c.467A>T MANE Select	NP_000468.1:p.Glu156Val