Canonical Allele Identifier: CA1468148850

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420272_73420273delinsGC , CM000666.2:g.73420272_73420273delinsGC	GRCh38
NC_000004.11:g.74285989_74285990delinsGC , CM000666.1:g.74285989_74285990delinsGC	GRCh37
NC_000004.10:g.74504853_74504854delinsGC	NCBI36
NG_009291.1:g.21018_21019delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1804_1805delinsGC MANE Select	ENSP00000295897.4:p.Ala602=
ENST00000295897.8:c.1804_1805delinsGC	ENSP00000295897.4:p.Ala602=
ENST00000401494.7:c.1459_1460delinsGC	ENSP00000384695.3:p.Ala487=
ENST00000415165.6:c.1228_1229delinsGC	ENSP00000401820.2:p.Ala410=
ENST00000476441.6:c.*1083_*1084delinsGC	ENSP00000423727.1:n.*1083_*1084delinsGC
ENST00000495173.1:n.112_113delinsGC
ENST00000503124.5:c.1354_1355delinsGC	ENSP00000421027.1:p.Ala452=
ENST00000505649.5:n.1351_1352delinsGC
ENST00000508932.5:n.194_195delinsGC
ENST00000509063.5:c.1785+633_1785+634delinsGC	ENSP00000422784.1:n.1785+633_1785+634deli...
ENST00000511370.1:c.1337_1338delinsGC
ENST00000621085.4:c.1165_1166delinsGC	ENSP00000483421.1:p.Ala389=
ENST00000621628.4:c.1165_1166delinsGC	ENSP00000480485.1:p.Ala389=
NM_000477.5:c.1804_1805delinsGC	NP_000468.1:p.Ala602=
NM_000477.6:c.1804_1805delinsGC	NP_000468.1:p.Ala602=
NM_000477.7:c.1804_1805delinsGC MANE Select	NP_000468.1:p.Ala602=