Canonical Allele Identifier: CA645517867

Gene: ALB

Linked Data

• COSMIC: COSM1633770

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418275_73418279del , CM000666.2:g.73418275_73418279del	GRCh38
NC_000004.11:g.74283992_74283996del , CM000666.1:g.74283992_74283996del	GRCh37
NC_000004.10:g.74502856_74502860del	NCBI36
NG_009291.1:g.19021_19025del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1616_1620del MANE Select	ENSP00000295897.4:p.Thr539IlefsTer2
ENST00000295897.8:c.1616_1620del	ENSP00000295897.4:p.Thr539IlefsTer2
ENST00000401494.7:c.1271_1275del	ENSP00000384695.3:p.Thr424IlefsTer2
ENST00000415165.6:c.1040_1044del	ENSP00000401820.2:p.Thr347IlefsTer2
ENST00000476441.6:c.*895_*899del	ENSP00000423727.1:n.*895_*899del
ENST00000486939.1:n.270_274del
ENST00000503124.5:c.1166_1170del	ENSP00000421027.1:p.Thr389IlefsTer2
ENST00000505649.5:n.1163_1167del
ENST00000509063.5:c.1616_1620del	ENSP00000422784.1:p.Thr539IlefsTer2
ENST00000511370.1:c.1149_1153del
ENST00000621085.4:c.977_981del	ENSP00000483421.1:p.Thr326IlefsTer2
ENST00000621628.4:c.977_981del	ENSP00000480485.1:p.Thr326IlefsTer2
NM_000477.5:c.1616_1620del	NP_000468.1:p.Thr539IlefsTer2
NM_000477.6:c.1616_1620del	NP_000468.1:p.Thr539IlefsTer2
NM_000477.7:c.1616_1620del MANE Select	NP_000468.1:p.Thr539IlefsTer2