Canonical Allele Identifier: CA2524521551

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406291_73406292insGT , CM000666.2:g.73406291_73406292insGT	GRCh38
NC_000004.11:g.74272008_74272009insGT , CM000666.1:g.74272008_74272009insGT	GRCh37
NC_000004.10:g.74490872_74490873insGT	NCBI36
NG_009291.1:g.7037_7038insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-338_138-337insGT MANE Select	ENSP00000295897.4:n.138-338_138-337insGT
ENST00000295897.8:c.138-338_138-337insGT	ENSP00000295897.4:n.138-338_138-337insGT
ENST00000401494.7:c.137+1118_137+1119insGT	ENSP00000384695.3:n.137+1118_137+1119insGT
ENST00000415165.6:c.137+1118_137+1119insGT	ENSP00000401820.2:n.137+1118_137+1119insGT
ENST00000441319.5:c.144-338_144-337insGT	ENSP00000392541.1:n.144-338_144-337insGT
ENST00000476441.6:c.79+1885_79+1886insGT	ENSP00000423727.1:n.79+1885_79+1886insGT
ENST00000503124.5:c.-101-338_-101-337insGT	ENSP00000421027.1:n.-101-338_-101-337insGT
ENST00000509063.5:c.138-338_138-337insGT	ENSP00000422784.1:n.138-338_138-337insGT
ENST00000510166.5:n.174-338_174-337insGT
ENST00000514786.1:n.107-338_107-337insGT
ENST00000515133.5:n.179-338_179-337insGT
ENST00000621085.4:c.138-338_138-337insGT	ENSP00000483421.1:n.138-338_138-337insGT
ENST00000621628.4:c.138-338_138-337insGT	ENSP00000480485.1:n.138-338_138-337insGT
NM_000477.5:c.138-338_138-337insGT	NP_000468.1:n.138-338_138-337insGT
NM_000477.6:c.138-338_138-337insGT	NP_000468.1:n.138-338_138-337insGT
NM_000477.7:c.138-338_138-337insGT MANE Select	NP_000468.1:n.138-338_138-337insGT