Canonical Allele Identifier: CA798289412

Gene: ALB

Linked Data

• dbSNP Id: rs1181240235
• gnomAD v3: 4-73413284-CAG-C
• gnomAD v4: 4-73413284-CAG-C
• MyVariant Identifiers: chr4:g.74279002_74279003del (hg19) ; chr4:g.73413285_73413286del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413287_73413288del , CM000666.2:g.73413287_73413288del	GRCh38
NC_000004.11:g.74279004_74279005del , CM000666.1:g.74279004_74279005del	GRCh37
NC_000004.10:g.74497868_74497869del	NCBI36
NG_009291.1:g.14033_14034del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-133_844-132del MANE Select	ENSP00000295897.4:n.844-133_844-132del
ENST00000295897.8:c.844-133_844-132del	ENSP00000295897.4:n.844-133_844-132del
ENST00000401494.7:c.499-133_499-132del	ENSP00000384695.3:n.499-133_499-132del
ENST00000415165.6:c.268-133_268-132del	ENSP00000401820.2:n.268-133_268-132del
ENST00000476441.6:c.*123-133_*123-132del	ENSP00000423727.1:n.*123-133_*123-132del
ENST00000484992.1:n.31_32del
ENST00000503124.5:c.394-133_394-132del	ENSP00000421027.1:n.394-133_394-132del
ENST00000505649.5:n.530-133_530-132del
ENST00000509063.5:c.844-133_844-132del	ENSP00000422784.1:n.844-133_844-132del
ENST00000511370.1:c.377-133_377-132del
ENST00000621085.4:c.491-1819_491-1818del	ENSP00000483421.1:n.491-1819_491-1818del
ENST00000621628.4:c.487-1815_487-1814del	ENSP00000480485.1:n.487-1815_487-1814del
NM_000477.5:c.844-133_844-132del	NP_000468.1:n.844-133_844-132del
NM_000477.6:c.844-133_844-132del	NP_000468.1:n.844-133_844-132del
NM_000477.7:c.844-133_844-132del MANE Select	NP_000468.1:n.844-133_844-132del