Canonical Allele Identifier: CA645517854

Gene: ALB

Linked Data

• COSMIC: COSM1727550

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415107_73415119del , CM000666.2:g.73415107_73415119del	GRCh38
NC_000004.11:g.74280824_74280836del , CM000666.1:g.74280824_74280836del	GRCh37
NC_000004.10:g.74499688_74499700del	NCBI36
NG_009291.1:g.15853_15865del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1131_1143del MANE Select	ENSP00000295897.4:p.Tyr377Ter
ENST00000295897.8:c.1131_1143del	ENSP00000295897.4:p.Tyr377Ter
ENST00000401494.7:c.786_798del	ENSP00000384695.3:p.Tyr262Ter
ENST00000415165.6:c.555_567del	ENSP00000401820.2:p.Tyr185Ter
ENST00000476441.6:c.*410_*422del	ENSP00000423727.1:n.*410_*422del
ENST00000484992.1:n.451_463del
ENST00000503124.5:c.681_693del	ENSP00000421027.1:p.Tyr227Ter
ENST00000504043.1:n.134_146del
ENST00000505649.5:n.817_829del
ENST00000509063.5:c.1131_1143del	ENSP00000422784.1:p.Tyr377Ter
ENST00000511370.1:c.664_676del
ENST00000621085.4:c.492_504del
ENST00000621628.4:c.492_504del	ENSP00000480485.1:p.Tyr164Ter
NM_000477.5:c.1131_1143del	NP_000468.1:p.Tyr377Ter
NM_000477.6:c.1131_1143del	NP_000468.1:p.Tyr377Ter
NM_000477.7:c.1131_1143del MANE Select	NP_000468.1:p.Tyr377Ter