Canonical Allele Identifier: CA1468148430
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404314_73404316delinsACG , CM000666.2:g.73404314_73404316delinsACG GRCh38
NC_000004.11:g.74270031_74270033delinsACG , CM000666.1:g.74270031_74270033delinsACG GRCh37
NC_000004.10:g.74488895_74488897delinsACG NCBI36
NG_009291.1:g.5060_5062delinsACG

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-14_-12delinsACG MANE Select ENSP00000295897.4:n.-14_-12delinsACG
ENST00000295897.8:c.-14_-12delinsACG ENSP00000295897.4:n.-14_-12delinsACG
ENST00000401494.7:c.-14_-12delinsACG ENSP00000384695.3:n.-14_-12delinsACG
ENST00000415165.6:c.-14_-12delinsACG ENSP00000401820.2:n.-14_-12delinsACG
ENST00000441319.5:n.48-55_48-53delinsACG ENSP00000392541.1:n.48-55_48-53delinsACG
ENST00000476441.6:c.-14_-12delinsACG ENSP00000423727.1:n.-14_-12delinsACG
ENST00000503124.5:c.-194_-192delinsACG ENSP00000421027.1:n.-194_-192delinsACG
ENST00000509063.5:c.-14_-12delinsACG ENSP00000422784.1:n.-14_-12delinsACG
ENST00000510166.5:n.28_30delinsACG
ENST00000514786.1:n.26_28delinsACG
ENST00000515133.5:n.28_30delinsACG
ENST00000621085.4:c.-14_-12delinsACG ENSP00000483421.1:n.-14_-12delinsACG
ENST00000621628.4:c.-14_-12delinsACG ENSP00000480485.1:n.-14_-12delinsACG
NM_000477.5:c.-14_-12delinsACG NP_000468.1:n.-14_-12delinsACG
NM_000477.6:c.-14_-12delinsACG NP_000468.1:n.-14_-12delinsACG
NM_000477.7:c.-14_-12delinsACG MANE Select NP_000468.1:n.-14_-12delinsACG