Canonical Allele Identifier: CA1468152575

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409172_73409174delinsCTT , CM000666.2:g.73409172_73409174delinsCTT	GRCh38
NC_000004.11:g.74274889_74274891delinsCTT , CM000666.1:g.74274889_74274891delinsCTT	GRCh37
NC_000004.10:g.74493753_74493755delinsCTT	NCBI36
NG_009291.1:g.9918_9920delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-183_483-181delinsCTT MANE Select	ENSP00000295897.4:n.483-183_483-181delinsCTT
ENST00000295897.8:c.483-183_483-181delinsCTT	ENSP00000295897.4:n.483-183_483-181delinsCTT
ENST00000401494.7:c.138-183_138-181delinsCTT	ENSP00000384695.3:n.138-183_138-181delinsCTT
ENST00000415165.6:c.138-2824_138-2822delinsCTT	ENSP00000401820.2:n.138-2824_138-2822delinsCTT
ENST00000441319.5:c.489-183_489-181delinsCTT	ENSP00000392541.1:n.489-183_489-181delinsCTT
ENST00000476441.6:c.80-183_80-181delinsCTT	ENSP00000423727.1:n.80-183_80-181delinsCTT
ENST00000503124.5:c.33-183_33-181delinsCTT	ENSP00000421027.1:n.33-183_33-181delinsCTT
ENST00000505649.5:n.169-183_169-181delinsCTT
ENST00000509063.5:c.483-183_483-181delinsCTT	ENSP00000422784.1:n.483-183_483-181delinsCTT
ENST00000514786.1:n.452-183_452-181delinsCTT
ENST00000621085.4:c.483-183_483-181delinsCTT	ENSP00000483421.1:n.483-183_483-181delinsCTT
ENST00000621628.4:c.486+96_486+98delinsCTT	ENSP00000480485.1:n.486+96_486+98delinsCTT
NM_000477.5:c.483-183_483-181delinsCTT	NP_000468.1:n.483-183_483-181delinsCTT
NM_000477.6:c.483-183_483-181delinsCTT	NP_000468.1:n.483-183_483-181delinsCTT
NM_000477.7:c.483-183_483-181delinsCTT MANE Select	NP_000468.1:n.483-183_483-181delinsCTT