Canonical Allele Identifier: CA2670965568

Gene: ALB

Linked Data

• gnomAD v4: 4-73415052-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415054del , CM000666.2:g.73415054del	GRCh38
NC_000004.11:g.74280771del , CM000666.1:g.74280771del	GRCh37
NC_000004.10:g.74499635del	NCBI36
NG_009291.1:g.15800del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1078del MANE Select	ENSP00000295897.4:p.Arg360GlufsTer12
ENST00000295897.8:c.1078del	ENSP00000295897.4:p.Arg360GlufsTer12
ENST00000401494.7:c.733del	ENSP00000384695.3:p.Arg245GlufsTer12
ENST00000415165.6:c.502del	ENSP00000401820.2:p.Arg168GlufsTer12
ENST00000476441.6:c.*357del	ENSP00000423727.1:n.*357del
ENST00000484992.1:n.398del
ENST00000503124.5:c.628del	ENSP00000421027.1:p.Arg210GlufsTer12
ENST00000504043.1:n.81del
ENST00000505649.5:n.764del
ENST00000509063.5:c.1078del	ENSP00000422784.1:p.Arg360GlufsTer12
ENST00000511370.1:c.611del
ENST00000621085.4:c.491-52del	ENSP00000483421.1:n.491-52del
ENST00000621628.4:c.487-48del	ENSP00000480485.1:n.487-48del
NM_000477.5:c.1078del	NP_000468.1:p.Arg360GlufsTer12
NM_000477.6:c.1078del	NP_000468.1:p.Arg360GlufsTer12
NM_000477.7:c.1078del MANE Select	NP_000468.1:p.Arg360GlufsTer12