Canonical Allele Identifier: CA552307243

Gene: ALB

Linked Data

• dbSNP Id: rs75000326
• gnomAD v2: 4-74285973-TA-T
• gnomAD v3: 4-73420256-TA-T
• gnomAD v4: 4-73420256-TA-T
• MyVariant Identifiers: chr4:g.74285974del (hg19) ; chr4:g.73420257del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420262del , CM000666.2:g.73420262del	GRCh38
NC_000004.11:g.74285979del , CM000666.1:g.74285979del	GRCh37
NC_000004.10:g.74504843del	NCBI36
NG_009291.1:g.21008del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1794del MANE Select	ENSP00000295897.4:p.Lys598AsnfsTer10
ENST00000295897.8:c.1794del	ENSP00000295897.4:p.Lys598AsnfsTer10
ENST00000401494.7:c.1449del	ENSP00000384695.3:p.Lys483AsnfsTer10
ENST00000415165.6:c.1218del	ENSP00000401820.2:p.Lys406AsnfsTer10
ENST00000476441.6:c.*1073del	ENSP00000423727.1:n.*1073del
ENST00000495173.1:n.102del
ENST00000503124.5:c.1344del	ENSP00000421027.1:p.Lys448AsnfsTer10
ENST00000505649.5:n.1341del
ENST00000508932.5:n.184del
ENST00000509063.5:c.1785+623del	ENSP00000422784.1:n.1785+623del
ENST00000511370.1:c.1327del
ENST00000621085.4:c.1155del	ENSP00000483421.1:p.Lys385AsnfsTer10
ENST00000621628.4:c.1155del	ENSP00000480485.1:p.Lys385AsnfsTer10
NM_000477.5:c.1794del	NP_000468.1:p.Lys598AsnfsTer10
NM_000477.6:c.1794del	NP_000468.1:p.Lys598AsnfsTer10
NM_000477.7:c.1794del MANE Select	NP_000468.1:p.Lys598AsnfsTer10