Canonical Allele Identifier: CA1468152632

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409274_73409275delinsCT , CM000666.2:g.73409274_73409275delinsCT	GRCh38
NC_000004.11:g.74274991_74274992delinsCT , CM000666.1:g.74274991_74274992delinsCT	GRCh37
NC_000004.10:g.74493855_74493856delinsCT	NCBI36
NG_009291.1:g.10020_10021delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-81_483-80delinsCT MANE Select	ENSP00000295897.4:n.483-81_483-80delinsCT...
ENST00000295897.8:c.483-81_483-80delinsCT	ENSP00000295897.4:n.483-81_483-80delinsCT...
ENST00000401494.7:c.138-81_138-80delinsCT	ENSP00000384695.3:n.138-81_138-80delinsCT...
ENST00000415165.6:c.138-2722_138-2721delinsCT	ENSP00000401820.2:n.138-2722_138-2721deli...
ENST00000441319.5:c.489-81_489-80delinsCT	ENSP00000392541.1:n.489-81_489-80delinsCT...
ENST00000476441.6:c.80-81_80-80delinsCT	ENSP00000423727.1:n.80-81_80-80delinsCT
ENST00000503124.5:c.33-81_33-80delinsCT	ENSP00000421027.1:n.33-81_33-80delinsCT
ENST00000505649.5:n.169-81_169-80delinsCT
ENST00000509063.5:c.483-81_483-80delinsCT	ENSP00000422784.1:n.483-81_483-80delinsCT...
ENST00000514786.1:n.452-81_452-80delinsCT
ENST00000621085.4:c.483-81_483-80delinsCT	ENSP00000483421.1:n.483-81_483-80delinsCT...
ENST00000621628.4:c.486+198_486+199delinsCT	ENSP00000480485.1:n.486+198_486+199delins...
NM_000477.5:c.483-81_483-80delinsCT	NP_000468.1:n.483-81_483-80delinsCT
NM_000477.6:c.483-81_483-80delinsCT	NP_000468.1:n.483-81_483-80delinsCT
NM_000477.7:c.483-81_483-80delinsCT MANE Select	NP_000468.1:n.483-81_483-80delinsCT