Canonical Allele Identifier: CA2959752

Gene: ALB

Linked Data

• dbSNP Id: rs769044962
• ExAC: 4:74285989 GC / G
• gnomAD v2: 4-74285989-GC-G
• gnomAD v3: 4-73420272-GC-G
• gnomAD v4: 4-73420272-GC-G
• MyVariant Identifiers: chr4:g.74285990del (hg19) ; chr4:g.73420273del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420273del , CM000666.2:g.73420273del	GRCh38
NC_000004.11:g.74285990del , CM000666.1:g.74285990del	GRCh37
NC_000004.10:g.74504854del	NCBI36
NG_009291.1:g.21019del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1805del MANE Select	ENSP00000295897.4:p.Ala602GlufsTer6
ENST00000295897.8:c.1805del	ENSP00000295897.4:p.Ala602GlufsTer6
ENST00000401494.7:c.1460del	ENSP00000384695.3:p.Ala487GlufsTer6
ENST00000415165.6:c.1229del	ENSP00000401820.2:p.Ala410GlufsTer6
ENST00000476441.6:c.*1084del	ENSP00000423727.1:n.*1084del
ENST00000495173.1:n.113del
ENST00000503124.5:c.1355del	ENSP00000421027.1:p.Ala452GlufsTer6
ENST00000505649.5:n.1352del
ENST00000508932.5:n.195del
ENST00000509063.5:c.1785+634del	ENSP00000422784.1:n.1785+634del
ENST00000511370.1:c.1338del
ENST00000621085.4:c.1166del	ENSP00000483421.1:p.Ala389GlufsTer6
ENST00000621628.4:c.1166del	ENSP00000480485.1:p.Ala389GlufsTer6
NM_000477.5:c.1805del	NP_000468.1:p.Ala602GlufsTer6
NM_000477.6:c.1805del	NP_000468.1:p.Ala602GlufsTer6
NM_000477.7:c.1805del MANE Select	NP_000468.1:p.Ala602GlufsTer6