Canonical Allele Identifier: CA1468148755

Gene: ALB

Linked Data

• dbSNP Id: rs1719109805
• gnomAD v4: 4-73420193-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420196_73420197del , CM000666.2:g.73420196_73420197del	GRCh38
NC_000004.11:g.74285913_74285914del , CM000666.1:g.74285913_74285914del	GRCh37
NC_000004.10:g.74504777_74504778del	NCBI36
NG_009291.1:g.20942_20943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-58_1786-57del MANE Select	ENSP00000295897.4:n.1786-58_1786-57del
ENST00000295897.8:c.1786-58_1786-57del	ENSP00000295897.4:n.1786-58_1786-57del
ENST00000401494.7:c.1441-58_1441-57del	ENSP00000384695.3:n.1441-58_1441-57del
ENST00000415165.6:c.1210-58_1210-57del	ENSP00000401820.2:n.1210-58_1210-57del
ENST00000476441.6:c.*1065-58_*1065-57del	ENSP00000423727.1:n.*1065-58_*1065-57del
ENST00000495173.1:n.94-58_94-57del
ENST00000503124.5:c.1336-58_1336-57del	ENSP00000421027.1:n.1336-58_1336-57del
ENST00000505649.5:n.1333-58_1333-57del
ENST00000508932.5:n.176-58_176-57del
ENST00000509063.5:c.1785+557_1785+558del	ENSP00000422784.1:n.1785+557_1785+558del
ENST00000511370.1:c.1319-58_1319-57del
ENST00000621085.4:c.1147-58_1147-57del	ENSP00000483421.1:n.1147-58_1147-57del
ENST00000621628.4:c.1147-58_1147-57del	ENSP00000480485.1:n.1147-58_1147-57del
NM_000477.5:c.1786-58_1786-57del	NP_000468.1:n.1786-58_1786-57del
NM_000477.6:c.1786-58_1786-57del	NP_000468.1:n.1786-58_1786-57del
NM_000477.7:c.1786-58_1786-57del MANE Select	NP_000468.1:n.1786-58_1786-57del