Canonical Allele Identifier: CA1468148482

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404347_73404350delinsTTTC , CM000666.2:g.73404347_73404350delinsTTTC	GRCh38
NC_000004.11:g.74270064_74270067delinsTTTC , CM000666.1:g.74270064_74270067delinsTTTC	GRCh37
NC_000004.10:g.74488928_74488931delinsTTTC	NCBI36
NG_009291.1:g.5093_5096delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.20_23delinsTTTC MANE Select	ENSP00000295897.4:p.Ile7=
ENST00000295897.8:c.20_23delinsTTTC	ENSP00000295897.4:p.Ile7=
ENST00000401494.7:c.20_23delinsTTTC	ENSP00000384695.3:p.Ile7=
ENST00000415165.6:c.20_23delinsTTTC	ENSP00000401820.2:p.Ile7=
ENST00000441319.5:c.48-22_48-19delinsTTTC	ENSP00000392541.1:n.48-22_48-19delinsTTTC
ENST00000476441.6:c.20_23delinsTTTC	ENSP00000423727.1:p.Ile7=
ENST00000503124.5:c.-161_-158delinsTTTC	ENSP00000421027.1:n.-161_-158delinsTTTC
ENST00000509063.5:c.20_23delinsTTTC	ENSP00000422784.1:p.Ile7=
ENST00000510166.5:n.61_64delinsTTTC
ENST00000514786.1:n.48+11_48+14delinsTTTC
ENST00000515133.5:n.61_64delinsTTTC
ENST00000621085.4:c.20_23delinsTTTC	ENSP00000483421.1:p.Ile7=
ENST00000621628.4:c.20_23delinsTTTC	ENSP00000480485.1:p.Ile7=
NM_000477.5:c.20_23delinsTTTC	NP_000468.1:p.Ile7=
NM_000477.6:c.20_23delinsTTTC	NP_000468.1:p.Ile7=
NM_000477.7:c.20_23delinsTTTC MANE Select	NP_000468.1:p.Ile7=