Canonical Allele Identifier: CA2562382331

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419789_73419791del , CM000666.2:g.73419789_73419791del	GRCh38
NC_000004.11:g.74285506_74285508del , CM000666.1:g.74285506_74285508del	GRCh37
NC_000004.10:g.74504370_74504372del	NCBI36
NG_009291.1:g.20535_20537del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+150_1785+152del MANE Select	ENSP00000295897.4:n.1785+150_1785+152del
ENST00000295897.8:c.1785+150_1785+152del	ENSP00000295897.4:n.1785+150_1785+152del
ENST00000401494.7:c.1440+150_1440+152del	ENSP00000384695.3:n.1440+150_1440+152del
ENST00000415165.6:c.1209+150_1209+152del	ENSP00000401820.2:n.1209+150_1209+152del
ENST00000476441.6:c.*1064+150_*1064+152del	ENSP00000423727.1:n.*1064+150_*1064+152del
ENST00000495173.1:n.93+150_93+152del
ENST00000503124.5:c.1335+150_1335+152del	ENSP00000421027.1:n.1335+150_1335+152del
ENST00000505649.5:n.1332+150_1332+152del
ENST00000508932.5:n.175+334_175+336del
ENST00000509063.5:c.1785+150_1785+152del	ENSP00000422784.1:n.1785+150_1785+152del
ENST00000511370.1:c.1318+150_1318+152del
ENST00000621085.4:c.1146+150_1146+152del	ENSP00000483421.1:n.1146+150_1146+152del
ENST00000621628.4:c.1146+150_1146+152del	ENSP00000480485.1:n.1146+150_1146+152del
NM_000477.5:c.1785+150_1785+152del	NP_000468.1:n.1785+150_1785+152del
NM_000477.6:c.1785+150_1785+152del	NP_000468.1:n.1785+150_1785+152del
NM_000477.7:c.1785+150_1785+152del MANE Select	NP_000468.1:n.1785+150_1785+152del