Canonical Allele Identifier: CA552614275

Gene: ALB

Linked Data

• dbSNP Id: rs1273211759
• gnomAD v2: 4-74274850-AT-A
• gnomAD v3: 4-73409133-AT-A
• gnomAD v4: 4-73409133-AT-A
• MyVariant Identifiers: chr4:g.74274851del (hg19) ; chr4:g.73409134del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409136del , CM000666.2:g.73409136del	GRCh38
NC_000004.11:g.74274853del , CM000666.1:g.74274853del	GRCh37
NC_000004.10:g.74493717del	NCBI36
NG_009291.1:g.9882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.483-219del MANE Select	ENSP00000295897.4:n.483-219del
ENST00000295897.8:c.483-219del	ENSP00000295897.4:n.483-219del
ENST00000401494.7:c.138-219del	ENSP00000384695.3:n.138-219del
ENST00000415165.6:c.138-2860del	ENSP00000401820.2:n.138-2860del
ENST00000441319.5:c.489-219del	ENSP00000392541.1:n.489-219del
ENST00000476441.6:c.80-219del	ENSP00000423727.1:n.80-219del
ENST00000503124.5:c.33-219del	ENSP00000421027.1:n.33-219del
ENST00000505649.5:n.169-219del
ENST00000509063.5:c.483-219del	ENSP00000422784.1:n.483-219del
ENST00000514786.1:n.452-219del
ENST00000621085.4:c.483-219del	ENSP00000483421.1:n.483-219del
ENST00000621628.4:c.486+60del	ENSP00000480485.1:n.486+60del
NM_000477.5:c.483-219del	NP_000468.1:n.483-219del
NM_000477.6:c.483-219del	NP_000468.1:n.483-219del
NM_000477.7:c.483-219del MANE Select	NP_000468.1:n.483-219del