Canonical Allele Identifier: CA1468150947

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406727_73406730delinsCTGA , CM000666.2:g.73406727_73406730delinsCTGA	GRCh38
NC_000004.11:g.74272444_74272447delinsCTGA , CM000666.1:g.74272444_74272447delinsCTGA	GRCh37
NC_000004.10:g.74491308_74491311delinsCTGA	NCBI36
NG_009291.1:g.7473_7476delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.236_239delinsCTGA MANE Select	ENSP00000295897.4:p.Ala79=
ENST00000295897.8:c.236_239delinsCTGA	ENSP00000295897.4:p.Ala79=
ENST00000401494.7:c.137+1554_137+1557delinsCTGA	ENSP00000384695.3:n.137+1554_137+1557delinsCTGA
ENST00000415165.6:c.137+1554_137+1557delinsCTGA	ENSP00000401820.2:n.137+1554_137+1557delinsCTGA
ENST00000441319.5:c.242_245delinsCTGA	ENSP00000392541.1:p.Ala81=
ENST00000476441.6:c.79+2321_79+2324delinsCTGA	ENSP00000423727.1:n.79+2321_79+2324delinsCTGA
ENST00000503124.5:c.-3_1delinsCTGA
ENST00000509063.5:c.236_239delinsCTGA	ENSP00000422784.1:p.Ala79=
ENST00000510166.5:n.272_275delinsCTGA
ENST00000514786.1:n.205_208delinsCTGA
ENST00000515133.5:n.277_280delinsCTGA
ENST00000621085.4:c.236_239delinsCTGA	ENSP00000483421.1:p.Ala79=
ENST00000621628.4:c.236_239delinsCTGA	ENSP00000480485.1:p.Ala79=
NM_000477.5:c.236_239delinsCTGA	NP_000468.1:p.Ala79=
NM_000477.6:c.236_239delinsCTGA	NP_000468.1:p.Ala79=
NM_000477.7:c.236_239delinsCTGA MANE Select	NP_000468.1:p.Ala79=