Canonical Allele Identifier: CA357235289

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272354T>G (hg19) ; chr4:g.73406637T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406637T>G , CM000666.2:g.73406637T>G	GRCh38
NC_000004.11:g.74272354T>G , CM000666.1:g.74272354T>G	GRCh37
NC_000004.10:g.74491218T>G	NCBI36
NG_009291.1:g.7383T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.146T>G MANE Select	ENSP00000295897.4:p.Ile49Ser
ENST00000295897.8:c.146T>G	ENSP00000295897.4:p.Ile49Ser
ENST00000401494.7:c.137+1464T>G	ENSP00000384695.3:n.137+1464T>G
ENST00000415165.6:c.137+1464T>G	ENSP00000401820.2:n.137+1464T>G
ENST00000441319.5:c.152T>G	ENSP00000392541.1:p.Ile51Ser
ENST00000476441.6:c.79+2231T>G	ENSP00000423727.1:n.79+2231T>G
ENST00000503124.5:c.-93T>G	ENSP00000421027.1:n.-93T>G
ENST00000509063.5:c.146T>G	ENSP00000422784.1:p.Ile49Ser
ENST00000510166.5:n.182T>G
ENST00000514786.1:n.115T>G
ENST00000515133.5:n.187T>G
ENST00000621085.4:c.146T>G	ENSP00000483421.1:p.Ile49Ser
ENST00000621628.4:c.146T>G	ENSP00000480485.1:p.Ile49Ser
NM_000477.5:c.146T>G	NP_000468.1:p.Ile49Ser
NM_000477.6:c.146T>G	NP_000468.1:p.Ile49Ser
NM_000477.7:c.146T>G MANE Select	NP_000468.1:p.Ile49Ser