Canonical Allele Identifier: CA357241160

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280790C>T (hg19) ; chr4:g.73415073C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415073C>T , CM000666.2:g.73415073C>T	GRCh38
NC_000004.11:g.74280790C>T , CM000666.1:g.74280790C>T	GRCh37
NC_000004.10:g.74499654C>T	NCBI36
NG_009291.1:g.15819C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1097C>T MANE Select	ENSP00000295897.4:p.Ser366Phe
ENST00000295897.8:c.1097C>T	ENSP00000295897.4:p.Ser366Phe
ENST00000401494.7:c.752C>T	ENSP00000384695.3:p.Ser251Phe
ENST00000415165.6:c.521C>T	ENSP00000401820.2:p.Ser174Phe
ENST00000476441.6:c.*376C>T	ENSP00000423727.1:n.*376C>T
ENST00000484992.1:n.417C>T
ENST00000503124.5:c.647C>T	ENSP00000421027.1:p.Ser216Phe
ENST00000504043.1:n.100C>T
ENST00000505649.5:n.783C>T
ENST00000509063.5:c.1097C>T	ENSP00000422784.1:p.Ser366Phe
ENST00000511370.1:c.630C>T
ENST00000621085.4:c.491-33C>T	ENSP00000483421.1:n.491-33C>T
ENST00000621628.4:c.487-29C>T	ENSP00000480485.1:n.487-29C>T
NM_000477.5:c.1097C>T	NP_000468.1:p.Ser366Phe
NM_000477.6:c.1097C>T	NP_000468.1:p.Ser366Phe
NM_000477.7:c.1097C>T MANE Select	NP_000468.1:p.Ser366Phe