Canonical Allele Identifier: CA552304987

Gene: ALB

Linked Data

• gnomAD v2: 4-74272846-A-ACC
• gnomAD v3: 4-73407129-A-ACC
• gnomAD v4: 4-73407129-A-ACC
• MyVariant Identifiers: chr4:g.74272846_74272847insCC (hg19) ; chr4:g.73407129_73407130insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73407129_73407130insCC , CM000666.2:g.73407129_73407130insCC	GRCh38
NC_000004.11:g.74272846_74272847insCC , CM000666.1:g.74272846_74272847insCC	GRCh37
NC_000004.10:g.74491710_74491711insCC	NCBI36
NG_009291.1:g.7875_7876insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.270+368_270+369insCC MANE Select	ENSP00000295897.4:n.270+368_270+369insCC
ENST00000295897.8:c.270+368_270+369insCC	ENSP00000295897.4:n.270+368_270+369insCC
ENST00000401494.7:c.137+1956_137+1957insCC	ENSP00000384695.3:n.137+1956_137+1957insCC
ENST00000415165.6:c.137+1956_137+1957insCC	ENSP00000401820.2:n.137+1956_137+1957insCC
ENST00000441319.5:c.276+368_276+369insCC	ENSP00000392541.1:n.276+368_276+369insCC
ENST00000476441.6:c.80-2226_80-2225insCC	ENSP00000423727.1:n.80-2226_80-2225insCC
ENST00000503124.5:c.32+368_32+369insCC	ENSP00000421027.1:n.32+368_32+369insCC
ENST00000509063.5:c.270+368_270+369insCC	ENSP00000422784.1:n.270+368_270+369insCC
ENST00000510166.5:n.306+368_306+369insCC
ENST00000514786.1:n.239+368_239+369insCC
ENST00000515133.5:n.311+368_311+369insCC
ENST00000621085.4:c.270+368_270+369insCC	ENSP00000483421.1:n.270+368_270+369insCC
ENST00000621628.4:c.270+368_270+369insCC	ENSP00000480485.1:n.270+368_270+369insCC
NM_000477.5:c.270+368_270+369insCC	NP_000468.1:n.270+368_270+369insCC
NM_000477.6:c.270+368_270+369insCC	NP_000468.1:n.270+368_270+369insCC
NM_000477.7:c.270+368_270+369insCC MANE Select	NP_000468.1:n.270+368_270+369insCC