Canonical Allele Identifier: CA645517876

Gene: ALB

Linked Data

• COSMIC: COSM6308305

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420265dup , CM000666.2:g.73420265dup	GRCh38
NC_000004.11:g.74285982dup , CM000666.1:g.74285982dup	GRCh37
NC_000004.10:g.74504846dup	NCBI36
NG_009291.1:g.21011dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1797dup MANE Select	ENSP00000295897.4:p.Val600CysfsTer29
ENST00000295897.8:c.1797dup	ENSP00000295897.4:p.Val600CysfsTer29
ENST00000401494.7:c.1452dup	ENSP00000384695.3:p.Val485CysfsTer29
ENST00000415165.6:c.1221dup	ENSP00000401820.2:p.Val408CysfsTer29
ENST00000476441.6:c.*1076dup	ENSP00000423727.1:n.*1076dup
ENST00000495173.1:n.105dup
ENST00000503124.5:c.1347dup	ENSP00000421027.1:p.Val450CysfsTer29
ENST00000505649.5:n.1344dup
ENST00000508932.5:n.187dup
ENST00000509063.5:c.1785+626dup	ENSP00000422784.1:n.1785+626dup
ENST00000511370.1:c.1330dup
ENST00000621085.4:c.1158dup	ENSP00000483421.1:p.Val387CysfsTer29
ENST00000621628.4:c.1158dup	ENSP00000480485.1:p.Val387CysfsTer29
NM_000477.5:c.1797dup	NP_000468.1:p.Val600CysfsTer29
NM_000477.6:c.1797dup	NP_000468.1:p.Val600CysfsTer29
NM_000477.7:c.1797dup MANE Select	NP_000468.1:p.Val600CysfsTer29