Canonical Allele Identifier: CA1468148753

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420193_73420195delinsATT , CM000666.2:g.73420193_73420195delinsATT	GRCh38
NC_000004.11:g.74285910_74285912delinsATT , CM000666.1:g.74285910_74285912delinsATT	GRCh37
NC_000004.10:g.74504774_74504776delinsATT	NCBI36
NG_009291.1:g.20939_20941delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-61_1786-59delinsATT MANE Select	ENSP00000295897.4:n.1786-61_1786-59delinsATT
ENST00000295897.8:c.1786-61_1786-59delinsATT	ENSP00000295897.4:n.1786-61_1786-59delinsATT
ENST00000401494.7:c.1441-61_1441-59delinsATT	ENSP00000384695.3:n.1441-61_1441-59delinsATT
ENST00000415165.6:c.1210-61_1210-59delinsATT	ENSP00000401820.2:n.1210-61_1210-59delinsATT
ENST00000476441.6:c.*1065-61_*1065-59delinsATT	ENSP00000423727.1:n.*1065-61_*1065-59delinsATT
ENST00000495173.1:n.94-61_94-59delinsATT
ENST00000503124.5:c.1336-61_1336-59delinsATT	ENSP00000421027.1:n.1336-61_1336-59delinsATT
ENST00000505649.5:n.1333-61_1333-59delinsATT
ENST00000508932.5:n.176-61_176-59delinsATT
ENST00000509063.5:c.1785+554_1785+556delinsATT	ENSP00000422784.1:n.1785+554_1785+556delinsATT
ENST00000511370.1:c.1319-61_1319-59delinsATT
ENST00000621085.4:c.1147-61_1147-59delinsATT	ENSP00000483421.1:n.1147-61_1147-59delinsATT
ENST00000621628.4:c.1147-61_1147-59delinsATT	ENSP00000480485.1:n.1147-61_1147-59delinsATT
NM_000477.5:c.1786-61_1786-59delinsATT	NP_000468.1:n.1786-61_1786-59delinsATT
NM_000477.6:c.1786-61_1786-59delinsATT	NP_000468.1:n.1786-61_1786-59delinsATT
NM_000477.7:c.1786-61_1786-59delinsATT MANE Select	NP_000468.1:n.1786-61_1786-59delinsATT