Canonical Allele Identifier: CA552304988

Gene: ALB

Linked Data

• dbSNP Id: rs1340740492
• gnomAD v2: 4-74272849-CCTTAACAT-C
• gnomAD v3: 4-73407132-CCTTAACAT-C
• gnomAD v4: 4-73407132-CCTTAACAT-C
• MyVariant Identifiers: chr4:g.74272850_74272857del (hg19) ; chr4:g.73407133_73407140del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407133_73407140del , CM000666.2:g.73407133_73407140del	GRCh38
NC_000004.11:g.74272850_74272857del , CM000666.1:g.74272850_74272857del	GRCh37
NC_000004.10:g.74491714_74491721del	NCBI36
NG_009291.1:g.7879_7886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+372_270+379del MANE Select	ENSP00000295897.4:n.270+372_270+379del
ENST00000295897.8:c.270+372_270+379del	ENSP00000295897.4:n.270+372_270+379del
ENST00000401494.7:c.137+1960_137+1967del	ENSP00000384695.3:n.137+1960_137+1967del
ENST00000415165.6:c.137+1960_137+1967del	ENSP00000401820.2:n.137+1960_137+1967del
ENST00000441319.5:c.276+372_276+379del	ENSP00000392541.1:n.276+372_276+379del
ENST00000476441.6:c.80-2222_80-2215del	ENSP00000423727.1:n.80-2222_80-2215del
ENST00000503124.5:c.32+372_32+379del	ENSP00000421027.1:n.32+372_32+379del
ENST00000509063.5:c.270+372_270+379del	ENSP00000422784.1:n.270+372_270+379del
ENST00000510166.5:n.306+372_306+379del
ENST00000514786.1:n.239+372_239+379del
ENST00000515133.5:n.311+372_311+379del
ENST00000621085.4:c.270+372_270+379del	ENSP00000483421.1:n.270+372_270+379del
ENST00000621628.4:c.270+372_270+379del	ENSP00000480485.1:n.270+372_270+379del
NM_000477.5:c.270+372_270+379del	NP_000468.1:n.270+372_270+379del
NM_000477.6:c.270+372_270+379del	NP_000468.1:n.270+372_270+379del
NM_000477.7:c.270+372_270+379del MANE Select	NP_000468.1:n.270+372_270+379del