Canonical Allele Identifier: CA917225968

Gene: ALB

Linked Data

• dbSNP Id: rs1577933585

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404361_73404362insG , CM000666.2:g.73404361_73404362insG	GRCh38
NC_000004.11:g.74270078_74270079insG , CM000666.1:g.74270078_74270079insG	GRCh37
NC_000004.10:g.74488942_74488943insG	NCBI36
NG_009291.1:g.5107_5108insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.34_35insG MANE Select	ENSP00000295897.4:p.Leu12ArgfsTer3
ENST00000295897.8:c.34_35insG	ENSP00000295897.4:p.Leu12ArgfsTer3
ENST00000401494.7:c.34_35insG	ENSP00000384695.3:p.Leu12ArgfsTer3
ENST00000415165.6:c.34_35insG	ENSP00000401820.2:p.Leu12ArgfsTer3
ENST00000441319.5:c.48-8_48-7insG	ENSP00000392541.1:n.48-8_48-7insG
ENST00000476441.6:c.34_35insG	ENSP00000423727.1:p.Leu12ArgfsTer3
ENST00000503124.5:c.-147_-146insG	ENSP00000421027.1:n.-147_-146insG
ENST00000509063.5:c.34_35insG	ENSP00000422784.1:p.Leu12ArgfsTer3
ENST00000510166.5:n.75_76insG
ENST00000514786.1:n.48+25_48+26insG
ENST00000515133.5:n.75_76insG
ENST00000621085.4:c.34_35insG	ENSP00000483421.1:p.Leu12ArgfsTer3
ENST00000621628.4:c.34_35insG	ENSP00000480485.1:p.Leu12ArgfsTer3
NM_000477.5:c.34_35insG	NP_000468.1:p.Leu12ArgfsTer3
NM_000477.6:c.34_35insG	NP_000468.1:p.Leu12ArgfsTer3
NM_000477.7:c.34_35insG MANE Select	NP_000468.1:p.Leu12ArgfsTer3