Canonical Allele Identifier: CA917225977
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1577933731

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404431_73404432insTGGGAGAA , CM000666.2:g.73404431_73404432insTGGGAGAA GRCh38
NC_000004.11:g.74270148_74270149insTGGGAGAA , CM000666.1:g.74270148_74270149insTGGGAGAA GRCh37
NC_000004.10:g.74489012_74489013insTGGGAGAA NCBI36
NG_009291.1:g.5177_5178insTGGGAGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.79+25_79+26insTGGGAGAA MANE Select ENSP00000295897.4:n.79+25_79+26insTGGGAGAA
ENST00000295897.8:c.79+25_79+26insTGGGAGAA ENSP00000295897.4:n.79+25_79+26insTGGGAGAA
ENST00000401494.7:c.79+25_79+26insTGGGAGAA ENSP00000384695.3:n.79+25_79+26insTGGGAGAA
ENST00000415165.6:c.79+25_79+26insTGGGAGAA ENSP00000401820.2:n.79+25_79+26insTGGGAGAA
ENST00000441319.5:c.85+25_85+26insTGGGAGAA ENSP00000392541.1:n.85+25_85+26insTGGGAGAA
ENST00000476441.6:c.79+25_79+26insTGGGAGAA ENSP00000423727.1:n.79+25_79+26insTGGGAGAA
ENST00000503124.5:c.-102+25_-102+26insTGGGAGAA ENSP00000421027.1:n.-102+25_-102+26insTGGGAGAA
ENST00000509063.5:c.79+25_79+26insTGGGAGAA ENSP00000422784.1:n.79+25_79+26insTGGGAGAA
ENST00000510166.5:n.120+25_120+26insTGGGAGAA
ENST00000514786.1:n.48+95_48+96insTGGGAGAA
ENST00000515133.5:n.120+25_120+26insTGGGAGAA
ENST00000621085.4:c.79+25_79+26insTGGGAGAA ENSP00000483421.1:n.79+25_79+26insTGGGAGAA
ENST00000621628.4:c.79+25_79+26insTGGGAGAA ENSP00000480485.1:n.79+25_79+26insTGGGAGAA
NM_000477.5:c.79+25_79+26insTGGGAGAA NP_000468.1:n.79+25_79+26insTGGGAGAA
NM_000477.6:c.79+25_79+26insTGGGAGAA NP_000468.1:n.79+25_79+26insTGGGAGAA
NM_000477.7:c.79+25_79+26insTGGGAGAA MANE Select NP_000468.1:n.79+25_79+26insTGGGAGAA