Canonical Allele Identifier: CA357241449

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280853C>T (hg19) ; chr4:g.73415136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415136C>T , CM000666.2:g.73415136C>T	GRCh38
NC_000004.11:g.74280853C>T , CM000666.1:g.74280853C>T	GRCh37
NC_000004.10:g.74499717C>T	NCBI36
NG_009291.1:g.15882C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1160C>T MANE Select	ENSP00000295897.4:p.Ala387Val
ENST00000295897.8:c.1160C>T	ENSP00000295897.4:p.Ala387Val
ENST00000401494.7:c.815C>T	ENSP00000384695.3:p.Ala272Val
ENST00000415165.6:c.584C>T	ENSP00000401820.2:p.Ala195Val
ENST00000476441.6:c.*439C>T	ENSP00000423727.1:n.*439C>T
ENST00000484992.1:n.480C>T
ENST00000503124.5:c.710C>T	ENSP00000421027.1:p.Ala237Val
ENST00000504043.1:n.163C>T
ENST00000505649.5:n.846C>T
ENST00000509063.5:c.1160C>T	ENSP00000422784.1:p.Ala387Val
ENST00000511370.1:c.693C>T
ENST00000621085.4:c.521C>T	ENSP00000483421.1:p.Ala174Val
ENST00000621628.4:c.521C>T	ENSP00000480485.1:p.Ala174Val
NM_000477.5:c.1160C>T	NP_000468.1:p.Ala387Val
NM_000477.6:c.1160C>T	NP_000468.1:p.Ala387Val
NM_000477.7:c.1160C>T MANE Select	NP_000468.1:p.Ala387Val