Canonical Allele Identifier: CA1468148861

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420277_73420278delinsTC , CM000666.2:g.73420277_73420278delinsTC	GRCh38
NC_000004.11:g.74285994_74285995delinsTC , CM000666.1:g.74285994_74285995delinsTC	GRCh37
NC_000004.10:g.74504858_74504859delinsTC	NCBI36
NG_009291.1:g.21023_21024delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1809_1810delinsTC MANE Select	ENSP00000295897.4:p.Ser603=
ENST00000295897.8:c.1809_1810delinsTC	ENSP00000295897.4:p.Ser603=
ENST00000401494.7:c.1464_1465delinsTC	ENSP00000384695.3:p.Ser488=
ENST00000415165.6:c.1233_1234delinsTC	ENSP00000401820.2:p.Ser411=
ENST00000476441.6:c.*1088_*1089delinsTC	ENSP00000423727.1:n.*1088_*1089delinsTC
ENST00000495173.1:n.117_118delinsTC
ENST00000503124.5:c.1359_1360delinsTC	ENSP00000421027.1:p.Ser453=
ENST00000505649.5:n.1356_1357delinsTC
ENST00000508932.5:n.199_200delinsTC
ENST00000509063.5:c.1785+638_1785+639delinsTC	ENSP00000422784.1:n.1785+638_1785+639delinsTC
ENST00000511370.1:c.1342_1343delinsTC
ENST00000621085.4:c.1170_1171delinsTC	ENSP00000483421.1:p.Ser390=
ENST00000621628.4:c.1170_1171delinsTC	ENSP00000480485.1:p.Ser390=
NM_000477.5:c.1809_1810delinsTC	NP_000468.1:p.Ser603=
NM_000477.6:c.1809_1810delinsTC	NP_000468.1:p.Ser603=
NM_000477.7:c.1809_1810delinsTC MANE Select	NP_000468.1:p.Ser603=