Canonical Allele Identifier: CA2670936828

Gene: ALB

Linked Data

• gnomAD v4: 4-73406567-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406568_73406569del , CM000666.2:g.73406568_73406569del	GRCh38
NC_000004.11:g.74272285_74272286del , CM000666.1:g.74272285_74272286del	GRCh37
NC_000004.10:g.74491149_74491150del	NCBI36
NG_009291.1:g.7314_7315del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-61_138-60del MANE Select	ENSP00000295897.4:n.138-61_138-60del
ENST00000295897.8:c.138-61_138-60del	ENSP00000295897.4:n.138-61_138-60del
ENST00000401494.7:c.137+1395_137+1396del	ENSP00000384695.3:n.137+1395_137+1396del
ENST00000415165.6:c.137+1395_137+1396del	ENSP00000401820.2:n.137+1395_137+1396del
ENST00000441319.5:c.144-61_144-60del	ENSP00000392541.1:n.144-61_144-60del
ENST00000476441.6:c.79+2162_79+2163del	ENSP00000423727.1:n.79+2162_79+2163del
ENST00000503124.5:c.-101-61_-101-60del	ENSP00000421027.1:n.-101-61_-101-60del
ENST00000509063.5:c.138-61_138-60del	ENSP00000422784.1:n.138-61_138-60del
ENST00000510166.5:n.174-61_174-60del
ENST00000514786.1:n.107-61_107-60del
ENST00000515133.5:n.179-61_179-60del
ENST00000621085.4:c.138-61_138-60del	ENSP00000483421.1:n.138-61_138-60del
ENST00000621628.4:c.138-61_138-60del	ENSP00000480485.1:n.138-61_138-60del
NM_000477.5:c.138-61_138-60del	NP_000468.1:n.138-61_138-60del
NM_000477.6:c.138-61_138-60del	NP_000468.1:n.138-61_138-60del
NM_000477.7:c.138-61_138-60del MANE Select	NP_000468.1:n.138-61_138-60del