Canonical Allele Identifier: CA2840611733

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419545del , CM000666.2:g.73419545del	GRCh38
NC_000004.11:g.74285262del , CM000666.1:g.74285262del	GRCh37
NC_000004.10:g.74504126del	NCBI36
NG_009291.1:g.20291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1691del MANE Select	ENSP00000295897.4:p.Thr564LysfsTer5
ENST00000295897.8:c.1691del	ENSP00000295897.4:p.Thr564LysfsTer5
ENST00000401494.7:c.1346del	ENSP00000384695.3:p.Thr449LysfsTer5
ENST00000415165.6:c.1115del	ENSP00000401820.2:p.Thr372LysfsTer5
ENST00000476441.6:c.*970del	ENSP00000423727.1:n.*970del
ENST00000486939.1:n.345del
ENST00000503124.5:c.1241del	ENSP00000421027.1:p.Thr414LysfsTer5
ENST00000505649.5:n.1238del
ENST00000508932.5:n.175+90del
ENST00000509063.5:c.1691del	ENSP00000422784.1:p.Thr564LysfsTer5
ENST00000511370.1:c.1224del
ENST00000621085.4:c.1052del	ENSP00000483421.1:p.Thr351LysfsTer5
ENST00000621628.4:c.1052del	ENSP00000480485.1:p.Thr351LysfsTer5
NM_000477.5:c.1691del	NP_000468.1:p.Thr564LysfsTer5
NM_000477.6:c.1691del	NP_000468.1:p.Thr564LysfsTer5
NM_000477.7:c.1691del MANE Select	NP_000468.1:p.Thr564LysfsTer5