Canonical Allele Identifier: CA648962886

Gene: ALB

Linked Data

• gnomAD v4: 4-73408939-AAAG-A
• COSMIC: COSN1300828 ; COSN1300829 ; COSN2044081

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408943_73408945del , CM000666.2:g.73408943_73408945del	GRCh38
NC_000004.11:g.74274660_74274662del , CM000666.1:g.74274660_74274662del	GRCh37
NC_000004.10:g.74493524_74493526del	NCBI36
NG_009291.1:g.9689_9691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+138_482+140del MANE Select	ENSP00000295897.4:n.482+138_482+140del
ENST00000295897.8:c.482+138_482+140del	ENSP00000295897.4:n.482+138_482+140del
ENST00000401494.7:c.138-412_138-410del	ENSP00000384695.3:n.138-412_138-410del
ENST00000415165.6:c.138-3053_138-3051del	ENSP00000401820.2:n.138-3053_138-3051del
ENST00000441319.5:c.488+138_488+140del	ENSP00000392541.1:n.488+138_488+140del
ENST00000476441.6:c.80-412_80-410del	ENSP00000423727.1:n.80-412_80-410del
ENST00000503124.5:c.33-412_33-410del	ENSP00000421027.1:n.33-412_33-410del
ENST00000505649.5:n.168+138_168+140del
ENST00000509063.5:c.482+138_482+140del	ENSP00000422784.1:n.482+138_482+140del
ENST00000514786.1:n.451+138_451+140del
ENST00000515133.5:n.661_663del
ENST00000621085.4:c.482+138_482+140del	ENSP00000483421.1:n.482+138_482+140del
ENST00000621628.4:c.483-130_483-128del	ENSP00000480485.1:n.483-130_483-128del
NM_000477.5:c.482+138_482+140del	NP_000468.1:n.482+138_482+140del
NM_000477.6:c.482+138_482+140del	NP_000468.1:n.482+138_482+140del
NM_000477.7:c.482+138_482+140del MANE Select	NP_000468.1:n.482+138_482+140del