Canonical Allele Identifier: CA357241104

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280773A>T (hg19) ; chr4:g.73415056A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415056A>T , CM000666.2:g.73415056A>T	GRCh38
NC_000004.11:g.74280773A>T , CM000666.1:g.74280773A>T	GRCh37
NC_000004.10:g.74499637A>T	NCBI36
NG_009291.1:g.15802A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1080A>T MANE Select	ENSP00000295897.4:p.Arg360Ser
ENST00000295897.8:c.1080A>T	ENSP00000295897.4:p.Arg360Ser
ENST00000401494.7:c.735A>T	ENSP00000384695.3:p.Arg245Ser
ENST00000415165.6:c.504A>T	ENSP00000401820.2:p.Arg168Ser
ENST00000476441.6:c.*359A>T	ENSP00000423727.1:n.*359A>T
ENST00000484992.1:n.400A>T
ENST00000503124.5:c.630A>T	ENSP00000421027.1:p.Arg210Ser
ENST00000504043.1:n.83A>T
ENST00000505649.5:n.766A>T
ENST00000509063.5:c.1080A>T	ENSP00000422784.1:p.Arg360Ser
ENST00000511370.1:c.613A>T
ENST00000621085.4:c.491-50A>T	ENSP00000483421.1:n.491-50A>T
ENST00000621628.4:c.487-46A>T	ENSP00000480485.1:n.487-46A>T
NM_000477.5:c.1080A>T	NP_000468.1:p.Arg360Ser
NM_000477.6:c.1080A>T	NP_000468.1:p.Arg360Ser
NM_000477.7:c.1080A>T MANE Select	NP_000468.1:p.Arg360Ser