Canonical Allele Identifier: CA645517853

Gene: ALB

Linked Data

• COSMIC: COSM5038631

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415102_73415124del , CM000666.2:g.73415102_73415124del	GRCh38
NC_000004.11:g.74280819_74280841del , CM000666.1:g.74280819_74280841del	GRCh37
NC_000004.10:g.74499683_74499705del	NCBI36
NG_009291.1:g.15848_15870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1126_1148del MANE Select	ENSP00000295897.4:p.Thr376ValfsTer9
ENST00000295897.8:c.1126_1148del	ENSP00000295897.4:p.Thr376ValfsTer9
ENST00000401494.7:c.781_803del	ENSP00000384695.3:p.Thr261ValfsTer9
ENST00000415165.6:c.550_572del	ENSP00000401820.2:p.Thr184ValfsTer9
ENST00000476441.6:c.*405_*427del	ENSP00000423727.1:n.*405_*427del
ENST00000484992.1:n.446_468del
ENST00000503124.5:c.676_698del	ENSP00000421027.1:p.Thr226ValfsTer9
ENST00000504043.1:n.129_151del
ENST00000505649.5:n.812_834del
ENST00000509063.5:c.1126_1148del	ENSP00000422784.1:p.Thr376ValfsTer9
ENST00000511370.1:c.659_681del
ENST00000621085.4:c.491-4_509del
ENST00000621628.4:c.487_509del	ENSP00000480485.1:p.Thr163ValfsTer9
NM_000477.5:c.1126_1148del	NP_000468.1:p.Thr376ValfsTer9
NM_000477.6:c.1126_1148del	NP_000468.1:p.Thr376ValfsTer9
NM_000477.7:c.1126_1148del MANE Select	NP_000468.1:p.Thr376ValfsTer9