Canonical Allele Identifier: CA2670936468

Gene: ALB

Linked Data

• gnomAD v4: 4-73404335-GGGTAACCTTTATTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404336_73404350del , CM000666.2:g.73404336_73404350del	GRCh38
NC_000004.11:g.74270053_74270067del , CM000666.1:g.74270053_74270067del	GRCh37
NC_000004.10:g.74488917_74488931del	NCBI36
NG_009291.1:g.5082_5096del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.9_23del MANE Select	ENSP00000295897.4:p.Trp3_Ser8delinsCys
ENST00000295897.8:c.9_23del	ENSP00000295897.4:p.Trp3_Ser8delinsCys
ENST00000401494.7:c.9_23del	ENSP00000384695.3:p.Trp3_Ser8delinsCys
ENST00000415165.6:c.9_23del	ENSP00000401820.2:p.Trp3_Ser8delinsCys
ENST00000441319.5:c.48-33_48-19del	ENSP00000392541.1:n.48-33_48-19del
ENST00000476441.6:c.9_23del	ENSP00000423727.1:p.Trp3_Ser8delinsCys
ENST00000503124.5:c.-172_-158del	ENSP00000421027.1:n.-172_-158del
ENST00000509063.5:c.9_23del	ENSP00000422784.1:p.Trp3_Ser8delinsCys
ENST00000510166.5:n.50_64del
ENST00000514786.1:n.48_48+14del
ENST00000515133.5:n.50_64del
ENST00000621085.4:c.9_23del	ENSP00000483421.1:p.Trp3_Ser8delinsCys
ENST00000621628.4:c.9_23del	ENSP00000480485.1:p.Trp3_Ser8delinsCys
NM_000477.5:c.9_23del	NP_000468.1:p.Trp3_Ser8delinsCys
NM_000477.6:c.9_23del	NP_000468.1:p.Trp3_Ser8delinsCys
NM_000477.7:c.9_23del MANE Select	NP_000468.1:p.Trp3_Ser8delinsCys