Canonical Allele Identifier: CA1468152529

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409085_73409088delinsGGTT , CM000666.2:g.73409085_73409088delinsGGTT	GRCh38
NC_000004.11:g.74274802_74274805delinsGGTT , CM000666.1:g.74274802_74274805delinsGGTT	GRCh37
NC_000004.10:g.74493666_74493669delinsGGTT	NCBI36
NG_009291.1:g.9831_9834delinsGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-270_483-267delinsGGTT MANE Select	ENSP00000295897.4:n.483-270_483-267delinsGGTT
ENST00000295897.8:c.483-270_483-267delinsGGTT	ENSP00000295897.4:n.483-270_483-267delinsGGTT
ENST00000401494.7:c.138-270_138-267delinsGGTT	ENSP00000384695.3:n.138-270_138-267delinsGGTT
ENST00000415165.6:c.138-2911_138-2908delinsGGTT	ENSP00000401820.2:n.138-2911_138-2908delinsGGTT
ENST00000441319.5:c.489-270_489-267delinsGGTT	ENSP00000392541.1:n.489-270_489-267delinsGGTT
ENST00000476441.6:c.80-270_80-267delinsGGTT	ENSP00000423727.1:n.80-270_80-267delinsGGTT
ENST00000503124.5:c.33-270_33-267delinsGGTT	ENSP00000421027.1:n.33-270_33-267delinsGGTT
ENST00000505649.5:n.169-270_169-267delinsGGTT
ENST00000509063.5:c.483-270_483-267delinsGGTT	ENSP00000422784.1:n.483-270_483-267delinsGGTT
ENST00000514786.1:n.452-270_452-267delinsGGTT
ENST00000621085.4:c.483-270_483-267delinsGGTT	ENSP00000483421.1:n.483-270_483-267delinsGGTT
ENST00000621628.4:c.486+9_486+12delinsGGTT	ENSP00000480485.1:n.486+9_486+12delinsGGTT
NM_000477.5:c.483-270_483-267delinsGGTT	NP_000468.1:n.483-270_483-267delinsGGTT
NM_000477.6:c.483-270_483-267delinsGGTT	NP_000468.1:n.483-270_483-267delinsGGTT
NM_000477.7:c.483-270_483-267delinsGGTT MANE Select	NP_000468.1:n.483-270_483-267delinsGGTT