Canonical Allele Identifier: CA99698122

Gene: ALB

Linked Data

• dbSNP Id: rs776480118
• gnomAD v2: 4-74271966-ACT-A
• gnomAD v3: 4-73406249-ACT-A
• gnomAD v4: 4-73406249-ACT-A
• MyVariant Identifiers: chr4:g.74271967_74271968del (hg19) ; chr4:g.73406250_73406251del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406252_73406253del , CM000666.2:g.73406252_73406253del	GRCh38
NC_000004.11:g.74271969_74271970del , CM000666.1:g.74271969_74271970del	GRCh37
NC_000004.10:g.74490833_74490834del	NCBI36
NG_009291.1:g.6998_6999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-377_138-376del MANE Select	ENSP00000295897.4:n.138-377_138-376del
ENST00000295897.8:c.138-377_138-376del	ENSP00000295897.4:n.138-377_138-376del
ENST00000401494.7:c.137+1079_137+1080del	ENSP00000384695.3:n.137+1079_137+1080del
ENST00000415165.6:c.137+1079_137+1080del	ENSP00000401820.2:n.137+1079_137+1080del
ENST00000441319.5:c.144-377_144-376del	ENSP00000392541.1:n.144-377_144-376del
ENST00000476441.6:c.79+1846_79+1847del	ENSP00000423727.1:n.79+1846_79+1847del
ENST00000503124.5:c.-101-377_-101-376del	ENSP00000421027.1:n.-101-377_-101-376del
ENST00000509063.5:c.138-377_138-376del	ENSP00000422784.1:n.138-377_138-376del
ENST00000510166.5:n.174-377_174-376del
ENST00000514786.1:n.107-377_107-376del
ENST00000515133.5:n.179-377_179-376del
ENST00000621085.4:c.138-377_138-376del	ENSP00000483421.1:n.138-377_138-376del
ENST00000621628.4:c.138-377_138-376del	ENSP00000480485.1:n.138-377_138-376del
NM_000477.5:c.138-377_138-376del	NP_000468.1:n.138-377_138-376del
NM_000477.6:c.138-377_138-376del	NP_000468.1:n.138-377_138-376del
NM_000477.7:c.138-377_138-376del MANE Select	NP_000468.1:n.138-377_138-376del