Canonical Allele Identifier: CA2739289687

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409388del , CM000666.2:g.73409388del	GRCh38
NC_000004.11:g.74275105del , CM000666.1:g.74275105del	GRCh37
NC_000004.10:g.74493969del	NCBI36
NG_009291.1:g.10134del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.516del MANE Select	ENSP00000295897.4:p.Tyr174MetfsTer?
ENST00000295897.8:c.516del	ENSP00000295897.4:p.Tyr174MetfsTer?
ENST00000401494.7:c.171del	ENSP00000384695.3:p.Tyr59MetfsTer?
ENST00000415165.6:c.138-2608del	ENSP00000401820.2:n.138-2608del
ENST00000441319.5:c.522del	ENSP00000392541.1:p.Tyr176MetfsTer?
ENST00000476441.6:c.113del	ENSP00000423727.1:p.Thr38IlefsTer11
ENST00000503124.5:c.66del	ENSP00000421027.1:p.Tyr24MetfsTer?
ENST00000505649.5:n.202del
ENST00000509063.5:c.516del	ENSP00000422784.1:p.Tyr174MetfsTer?
ENST00000511370.1:c.49del
ENST00000514786.1:n.485del
ENST00000621085.4:c.490+26del	ENSP00000483421.1:n.490+26del
ENST00000621628.4:c.486+312del	ENSP00000480485.1:n.486+312del
NM_000477.5:c.516del	NP_000468.1:p.Tyr174MetfsTer?
NM_000477.6:c.516del	NP_000468.1:p.Tyr174MetfsTer?
NM_000477.7:c.516del MANE Select	NP_000468.1:p.Tyr174MetfsTer?