Canonical Allele Identifier: CA357241138

Gene: ALB

Linked Data

• COSMIC: COSM1057404
• MyVariant Identifiers: chr4:g.74280785T>A (hg19) ; chr4:g.73415068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415068T>A , CM000666.2:g.73415068T>A	GRCh38
NC_000004.11:g.74280785T>A , CM000666.1:g.74280785T>A	GRCh37
NC_000004.10:g.74499649T>A	NCBI36
NG_009291.1:g.15814T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1092T>A MANE Select	ENSP00000295897.4:p.Asp364Glu
ENST00000295897.8:c.1092T>A	ENSP00000295897.4:p.Asp364Glu
ENST00000401494.7:c.747T>A	ENSP00000384695.3:p.Asp249Glu
ENST00000415165.6:c.516T>A	ENSP00000401820.2:p.Asp172Glu
ENST00000476441.6:c.*371T>A	ENSP00000423727.1:n.*371T>A
ENST00000484992.1:n.412T>A
ENST00000503124.5:c.642T>A	ENSP00000421027.1:p.Asp214Glu
ENST00000504043.1:n.95T>A
ENST00000505649.5:n.778T>A
ENST00000509063.5:c.1092T>A	ENSP00000422784.1:p.Asp364Glu
ENST00000511370.1:c.625T>A
ENST00000621085.4:c.491-38T>A	ENSP00000483421.1:n.491-38T>A
ENST00000621628.4:c.487-34T>A	ENSP00000480485.1:n.487-34T>A
NM_000477.5:c.1092T>A	NP_000468.1:p.Asp364Glu
NM_000477.6:c.1092T>A	NP_000468.1:p.Asp364Glu
NM_000477.7:c.1092T>A MANE Select	NP_000468.1:p.Asp364Glu