Canonical Allele Identifier: CA1468152456

Gene: ALB

Linked Data

• dbSNP Id: rs1718800239
• gnomAD v4: 4-73408932-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408938del , CM000666.2:g.73408938del	GRCh38
NC_000004.11:g.74274655del , CM000666.1:g.74274655del	GRCh37
NC_000004.10:g.74493519del	NCBI36
NG_009291.1:g.9684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+133del MANE Select	ENSP00000295897.4:n.482+133del
ENST00000295897.8:c.482+133del	ENSP00000295897.4:n.482+133del
ENST00000401494.7:c.138-417del	ENSP00000384695.3:n.138-417del
ENST00000415165.6:c.138-3058del	ENSP00000401820.2:n.138-3058del
ENST00000441319.5:c.488+133del	ENSP00000392541.1:n.488+133del
ENST00000476441.6:c.80-417del	ENSP00000423727.1:n.80-417del
ENST00000503124.5:c.33-417del	ENSP00000421027.1:n.33-417del
ENST00000505649.5:n.168+133del
ENST00000509063.5:c.482+133del	ENSP00000422784.1:n.482+133del
ENST00000514786.1:n.451+133del
ENST00000515133.5:n.656del
ENST00000621085.4:c.482+133del	ENSP00000483421.1:n.482+133del
ENST00000621628.4:c.482+133del	ENSP00000480485.1:n.482+133del
NM_000477.5:c.482+133del	NP_000468.1:n.482+133del
NM_000477.6:c.482+133del	NP_000468.1:n.482+133del
NM_000477.7:c.482+133del MANE Select	NP_000468.1:n.482+133del