Canonical Allele Identifier: CA2670966606

Gene: ALB

Linked Data

• gnomAD v4: 4-73419537-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419539del , CM000666.2:g.73419539del	GRCh38
NC_000004.11:g.74285256del , CM000666.1:g.74285256del	GRCh37
NC_000004.10:g.74504120del	NCBI36
NG_009291.1:g.20285del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1685del MANE Select	ENSP00000295897.4:p.Lys562ArgfsTer7
ENST00000295897.8:c.1685del	ENSP00000295897.4:p.Lys562ArgfsTer7
ENST00000401494.7:c.1340del	ENSP00000384695.3:p.Lys447ArgfsTer7
ENST00000415165.6:c.1109del	ENSP00000401820.2:p.Lys370ArgfsTer7
ENST00000476441.6:c.*964del	ENSP00000423727.1:n.*964del
ENST00000486939.1:n.339del
ENST00000503124.5:c.1235del	ENSP00000421027.1:p.Lys412ArgfsTer7
ENST00000505649.5:n.1232del
ENST00000508932.5:n.175+84del
ENST00000509063.5:c.1685del	ENSP00000422784.1:p.Lys562ArgfsTer7
ENST00000511370.1:c.1218del
ENST00000621085.4:c.1046del	ENSP00000483421.1:p.Lys349ArgfsTer7
ENST00000621628.4:c.1046del	ENSP00000480485.1:p.Lys349ArgfsTer7
NM_000477.5:c.1685del	NP_000468.1:p.Lys562ArgfsTer7
NM_000477.6:c.1685del	NP_000468.1:p.Lys562ArgfsTer7
NM_000477.7:c.1685del MANE Select	NP_000468.1:p.Lys562ArgfsTer7