Canonical Allele Identifier: CA1468146955

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418265_73418266delinsGA , CM000666.2:g.73418265_73418266delinsGA	GRCh38
NC_000004.11:g.74283982_74283983delinsGA , CM000666.1:g.74283982_74283983delinsGA	GRCh37
NC_000004.10:g.74502846_74502847delinsGA	NCBI36
NG_009291.1:g.19011_19012delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1606_1607delinsGA MANE Select	ENSP00000295897.4:p.Asp536=
ENST00000295897.8:c.1606_1607delinsGA	ENSP00000295897.4:p.Asp536=
ENST00000401494.7:c.1261_1262delinsGA	ENSP00000384695.3:p.Asp421=
ENST00000415165.6:c.1030_1031delinsGA	ENSP00000401820.2:p.Asp344=
ENST00000476441.6:c.*885_*886delinsGA	ENSP00000423727.1:n.*885_*886delinsGA
ENST00000486939.1:n.260_261delinsGA
ENST00000503124.5:c.1156_1157delinsGA	ENSP00000421027.1:p.Asp386=
ENST00000505649.5:n.1153_1154delinsGA
ENST00000509063.5:c.1606_1607delinsGA	ENSP00000422784.1:p.Asp536=
ENST00000511370.1:c.1139_1140delinsGA
ENST00000621085.4:c.967_968delinsGA	ENSP00000483421.1:p.Asp323=
ENST00000621628.4:c.967_968delinsGA	ENSP00000480485.1:p.Asp323=
NM_000477.5:c.1606_1607delinsGA	NP_000468.1:p.Asp536=
NM_000477.6:c.1606_1607delinsGA	NP_000468.1:p.Asp536=
NM_000477.7:c.1606_1607delinsGA MANE Select	NP_000468.1:p.Asp536=