Canonical Allele Identifier: CA1468150792

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406598_73406599delinsAT , CM000666.2:g.73406598_73406599delinsAT	GRCh38
NC_000004.11:g.74272315_74272316delinsAT , CM000666.1:g.74272315_74272316delinsAT	GRCh37
NC_000004.10:g.74491179_74491180delinsAT	NCBI36
NG_009291.1:g.7344_7345delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-31_138-30delinsAT MANE Select	ENSP00000295897.4:n.138-31_138-30delinsAT
ENST00000295897.8:c.138-31_138-30delinsAT	ENSP00000295897.4:n.138-31_138-30delinsAT
ENST00000401494.7:c.137+1425_137+1426delinsAT	ENSP00000384695.3:n.137+1425_137+1426delinsAT
ENST00000415165.6:c.137+1425_137+1426delinsAT	ENSP00000401820.2:n.137+1425_137+1426delinsAT
ENST00000441319.5:c.144-31_144-30delinsAT	ENSP00000392541.1:n.144-31_144-30delinsAT
ENST00000476441.6:c.79+2192_79+2193delinsAT	ENSP00000423727.1:n.79+2192_79+2193delinsAT
ENST00000503124.5:c.-101-31_-101-30delinsAT	ENSP00000421027.1:n.-101-31_-101-30delinsAT
ENST00000509063.5:c.138-31_138-30delinsAT	ENSP00000422784.1:n.138-31_138-30delinsAT
ENST00000510166.5:n.174-31_174-30delinsAT
ENST00000514786.1:n.107-31_107-30delinsAT
ENST00000515133.5:n.179-31_179-30delinsAT
ENST00000621085.4:c.138-31_138-30delinsAT	ENSP00000483421.1:n.138-31_138-30delinsAT
ENST00000621628.4:c.138-31_138-30delinsAT	ENSP00000480485.1:n.138-31_138-30delinsAT
NM_000477.5:c.138-31_138-30delinsAT	NP_000468.1:n.138-31_138-30delinsAT
NM_000477.6:c.138-31_138-30delinsAT	NP_000468.1:n.138-31_138-30delinsAT
NM_000477.7:c.138-31_138-30delinsAT MANE Select	NP_000468.1:n.138-31_138-30delinsAT