Canonical Allele Identifier: CA2706481623
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs2149327058

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406763_73406764insTGC , CM000666.2:g.73406763_73406764insTGC GRCh38
NC_000004.11:g.74272480_74272481insTGC , CM000666.1:g.74272480_74272481insTGC GRCh37
NC_000004.10:g.74491344_74491345insTGC NCBI36
NG_009291.1:g.7509_7510insTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.270+2_270+3insTGC MANE Select ENSP00000295897.4:n.270+2_270+3insTGC
ENST00000295897.8:c.270+2_270+3insTGC ENSP00000295897.4:n.270+2_270+3insTGC
ENST00000401494.7:c.137+1590_137+1591insTGC ENSP00000384695.3:n.137+1590_137+1591insTGC
ENST00000415165.6:c.137+1590_137+1591insTGC ENSP00000401820.2:n.137+1590_137+1591insTGC
ENST00000441319.5:c.276+2_276+3insTGC ENSP00000392541.1:n.276+2_276+3insTGC
ENST00000476441.6:c.79+2357_79+2358insTGC ENSP00000423727.1:n.79+2357_79+2358insTGC
ENST00000503124.5:c.32+2_32+3insTGC ENSP00000421027.1:n.32+2_32+3insTGC
ENST00000509063.5:c.270+2_270+3insTGC ENSP00000422784.1:n.270+2_270+3insTGC
ENST00000510166.5:n.306+2_306+3insTGC
ENST00000514786.1:n.239+2_239+3insTGC
ENST00000515133.5:n.311+2_311+3insTGC
ENST00000621085.4:c.270+2_270+3insTGC ENSP00000483421.1:n.270+2_270+3insTGC
ENST00000621628.4:c.270+2_270+3insTGC ENSP00000480485.1:n.270+2_270+3insTGC
NM_000477.5:c.270+2_270+3insTGC NP_000468.1:n.270+2_270+3insTGC
NM_000477.6:c.270+2_270+3insTGC NP_000468.1:n.270+2_270+3insTGC
NM_000477.7:c.270+2_270+3insTGC MANE Select NP_000468.1:n.270+2_270+3insTGC