Canonical Allele Identifier: CA99699021

Gene: ALB

Linked Data

• dbSNP Id: rs1001405633
• gnomAD v2: 4-74272807-G-GTATT
• gnomAD v3: 4-73407090-G-GTATT
• gnomAD v4: 4-73407090-G-GTATT
• MyVariant Identifiers: chr4:g.74272811_74272812insTATT (hg19) ; chr4:g.74272807_74272808insTATT (hg19) ; chr4:g.73407094_73407095insTATT (hg38) ; chr4:g.73407090_73407091insTATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407106_73407109dup , CM000666.2:g.73407106_73407109dup	GRCh38
NC_000004.11:g.74272823_74272826dup , CM000666.1:g.74272823_74272826dup	GRCh37
NC_000004.10:g.74491687_74491690dup	NCBI36
NG_009291.1:g.7852_7855dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+345_270+348dup MANE Select	ENSP00000295897.4:n.270+345_270+348dup
ENST00000295897.8:c.270+345_270+348dup	ENSP00000295897.4:n.270+345_270+348dup
ENST00000401494.7:c.137+1933_137+1936dup	ENSP00000384695.3:n.137+1933_137+1936dup
ENST00000415165.6:c.137+1933_137+1936dup	ENSP00000401820.2:n.137+1933_137+1936dup
ENST00000441319.5:c.276+345_276+348dup	ENSP00000392541.1:n.276+345_276+348dup
ENST00000476441.6:c.80-2249_80-2246dup	ENSP00000423727.1:n.80-2249_80-2246dup
ENST00000503124.5:c.32+345_32+348dup	ENSP00000421027.1:n.32+345_32+348dup
ENST00000509063.5:c.270+345_270+348dup	ENSP00000422784.1:n.270+345_270+348dup
ENST00000510166.5:n.306+345_306+348dup
ENST00000514786.1:n.239+345_239+348dup
ENST00000515133.5:n.311+345_311+348dup
ENST00000621085.4:c.270+345_270+348dup	ENSP00000483421.1:n.270+345_270+348dup
ENST00000621628.4:c.270+345_270+348dup	ENSP00000480485.1:n.270+345_270+348dup
NM_000477.5:c.270+345_270+348dup	NP_000468.1:n.270+345_270+348dup
NM_000477.6:c.270+345_270+348dup	NP_000468.1:n.270+345_270+348dup
NM_000477.7:c.270+345_270+348dup MANE Select	NP_000468.1:n.270+345_270+348dup