Canonical Allele Identifier: CA1468148596

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419947_73419948delinsTA , CM000666.2:g.73419947_73419948delinsTA	GRCh38
NC_000004.11:g.74285664_74285665delinsTA , CM000666.1:g.74285664_74285665delinsTA	GRCh37
NC_000004.10:g.74504528_74504529delinsTA	NCBI36
NG_009291.1:g.20693_20694delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-307_1786-306delinsTA MANE Select	ENSP00000295897.4:n.1786-307_1786-306delinsTA
ENST00000295897.8:c.1786-307_1786-306delinsTA	ENSP00000295897.4:n.1786-307_1786-306delinsTA
ENST00000401494.7:c.1441-307_1441-306delinsTA	ENSP00000384695.3:n.1441-307_1441-306delinsTA
ENST00000415165.6:c.1210-307_1210-306delinsTA	ENSP00000401820.2:n.1210-307_1210-306delinsTA
ENST00000476441.6:c.*1065-307_*1065-306delinsTA	ENSP00000423727.1:n.*1065-307_*1065-306delinsTA
ENST00000495173.1:n.94-307_94-306delinsTA
ENST00000503124.5:c.1336-307_1336-306delinsTA	ENSP00000421027.1:n.1336-307_1336-306delinsTA
ENST00000505649.5:n.1333-307_1333-306delinsTA
ENST00000508932.5:n.176-307_176-306delinsTA
ENST00000509063.5:c.1785+308_1785+309delinsTA	ENSP00000422784.1:n.1785+308_1785+309delinsTA
ENST00000511370.1:c.1319-307_1319-306delinsTA
ENST00000621085.4:c.1147-307_1147-306delinsTA	ENSP00000483421.1:n.1147-307_1147-306delinsTA
ENST00000621628.4:c.1147-307_1147-306delinsTA	ENSP00000480485.1:n.1147-307_1147-306delinsTA
NM_000477.5:c.1786-307_1786-306delinsTA	NP_000468.1:n.1786-307_1786-306delinsTA
NM_000477.6:c.1786-307_1786-306delinsTA	NP_000468.1:n.1786-307_1786-306delinsTA
NM_000477.7:c.1786-307_1786-306delinsTA MANE Select	NP_000468.1:n.1786-307_1786-306delinsTA