Canonical Allele Identifier: CA1468152311

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408600_73408601delinsCT , CM000666.2:g.73408600_73408601delinsCT	GRCh38
NC_000004.11:g.74274317_74274318delinsCT , CM000666.1:g.74274317_74274318delinsCT	GRCh37
NC_000004.10:g.74493181_74493182delinsCT	NCBI36
NG_009291.1:g.9346_9347delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.277_278delinsCT MANE Select	ENSP00000295897.4:p.Leu93=
ENST00000295897.8:c.277_278delinsCT	ENSP00000295897.4:p.Leu93=
ENST00000401494.7:c.138-755_138-754delinsCT	ENSP00000384695.3:n.138-755_138-754delinsCT
ENST00000415165.6:c.138-3396_138-3395delinsCT	ENSP00000401820.2:n.138-3396_138-3395delinsCT
ENST00000441319.5:c.283_284delinsCT	ENSP00000392541.1:p.Leu95=
ENST00000476441.6:c.80-755_80-754delinsCT	ENSP00000423727.1:n.80-755_80-754delinsCT
ENST00000503124.5:c.33-755_33-754delinsCT	ENSP00000421027.1:n.33-755_33-754delinsCT
ENST00000509063.5:c.277_278delinsCT	ENSP00000422784.1:p.Leu93=
ENST00000510166.5:n.313_314delinsCT
ENST00000514786.1:n.246_247delinsCT
ENST00000515133.5:n.318_319delinsCT
ENST00000621085.4:c.277_278delinsCT	ENSP00000483421.1:p.Leu93=
ENST00000621628.4:c.277_278delinsCT	ENSP00000480485.1:p.Leu93=
NM_000477.5:c.277_278delinsCT	NP_000468.1:p.Leu93=
NM_000477.6:c.277_278delinsCT	NP_000468.1:p.Leu93=
NM_000477.7:c.277_278delinsCT MANE Select	NP_000468.1:p.Leu93=