Canonical Allele Identifier: CA1468148586

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419936_73419941delinsATTAAT , CM000666.2:g.73419936_73419941delinsATTAAT	GRCh38
NC_000004.11:g.74285653_74285658delinsATTAAT , CM000666.1:g.74285653_74285658delinsATTAAT	GRCh37
NC_000004.10:g.74504517_74504522delinsATTAAT	NCBI36
NG_009291.1:g.20682_20687delinsATTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+297_1785+302delinsATTAAT MANE Select	ENSP00000295897.4:n.1785+297_1785+302delinsATTAAT
ENST00000295897.8:c.1785+297_1785+302delinsATTAAT	ENSP00000295897.4:n.1785+297_1785+302delinsATTAAT
ENST00000401494.7:c.1440+297_1440+302delinsATTAAT	ENSP00000384695.3:n.1440+297_1440+302delinsATTAAT
ENST00000415165.6:c.1209+297_1209+302delinsATTAAT	ENSP00000401820.2:n.1209+297_1209+302delinsATTAAT
ENST00000476441.6:c.*1064+297_*1064+302delinsATTAAT	ENSP00000423727.1:n.*1064+297_*1064+302delinsATTAAT
ENST00000495173.1:n.93+297_93+302delinsATTAAT
ENST00000503124.5:c.1335+297_1335+302delinsATTAAT	ENSP00000421027.1:n.1335+297_1335+302delinsATTAAT
ENST00000505649.5:n.1332+297_1332+302delinsATTAAT
ENST00000508932.5:n.176-318_176-313delinsATTAAT
ENST00000509063.5:c.1785+297_1785+302delinsATTAAT	ENSP00000422784.1:n.1785+297_1785+302delinsATTAAT
ENST00000511370.1:c.1318+297_1318+302delinsATTAAT
ENST00000621085.4:c.1146+297_1146+302delinsATTAAT	ENSP00000483421.1:n.1146+297_1146+302delinsATTAAT
ENST00000621628.4:c.1146+297_1146+302delinsATTAAT	ENSP00000480485.1:n.1146+297_1146+302delinsATTAAT
NM_000477.5:c.1785+297_1785+302delinsATTAAT	NP_000468.1:n.1785+297_1785+302delinsATTAAT
NM_000477.6:c.1785+297_1785+302delinsATTAAT	NP_000468.1:n.1785+297_1785+302delinsATTAAT
NM_000477.7:c.1785+297_1785+302delinsATTAAT MANE Select	NP_000468.1:n.1785+297_1785+302delinsATTAAT