Canonical Allele Identifier: CA2580071800

Gene: ALB

Linked Data

• ClinVar Variation Id: 18211
• ClinVar RCV Id: RCV000019870

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420293_73420322delinsAAAAT , CM000666.2:g.73420293_73420322delinsAAAAT	GRCh38
NC_000004.11:g.74286010_74286039delinsAAAAT , CM000666.1:g.74286010_74286039delinsAAAAT	GRCh37
NC_000004.10:g.74504874_74504903delinsAAAAT	NCBI36
NG_009291.1:g.21039_21068delinsAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1825_*23+1delinsAAAAT
ENST00000295897.8:c.1825_*23+1delinsAAAAT
ENST00000401494.7:c.1480_*23+1delinsAAAAT
ENST00000415165.6:c.1249_*23+1delinsAAAAT
ENST00000476441.6:c.*1104_*1132+1delinsAAAAT
ENST00000495173.1:n.133_161+1delinsAAAAT
ENST00000503124.5:c.1375_*23+1delinsAAAAT
ENST00000505649.5:n.1372_1400+1delinsAAAAT
ENST00000508932.5:n.215_243+1delinsAAAAT
ENST00000509063.5:c.1785+654_1785+683delinsAAAAT	ENSP00000422784.1:n.1785+654_1785+683delinsAAAAT
ENST00000511370.1:c.1358_1386+1delinsAAAAT
ENST00000621085.4:c.1186_*23+1delinsAAAAT
ENST00000621628.4:c.1186_*23+1delinsAAAAT
NM_000477.5:c.1825_*23+1delinsAAAAT
NM_000477.6:c.1825_*23+1delinsAAAAT
NM_000477.7:c.1825_*23+1delinsAAAAT