Canonical Allele Identifier: CA1468148668
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404418_73404422delinsATTTT , CM000666.2:g.73404418_73404422delinsATTTT GRCh38
NC_000004.11:g.74270135_74270139delinsATTTT , CM000666.1:g.74270135_74270139delinsATTTT GRCh37
NC_000004.10:g.74488999_74489003delinsATTTT NCBI36
NG_009291.1:g.5164_5168delinsATTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.79+12_79+16delinsATTTT MANE Select ENSP00000295897.4:n.79+12_79+16delinsATTT...
ENST00000295897.8:c.79+12_79+16delinsATTTT ENSP00000295897.4:n.79+12_79+16delinsATTT...
ENST00000401494.7:c.79+12_79+16delinsATTTT ENSP00000384695.3:n.79+12_79+16delinsATTT...
ENST00000415165.6:c.79+12_79+16delinsATTTT ENSP00000401820.2:n.79+12_79+16delinsATTT...
ENST00000441319.5:c.85+12_85+16delinsATTTT ENSP00000392541.1:n.85+12_85+16delinsATTT...
ENST00000476441.6:c.79+12_79+16delinsATTTT ENSP00000423727.1:n.79+12_79+16delinsATTT...
ENST00000503124.5:c.-102+12_-102+16delinsATTTT ENSP00000421027.1:n.-102+12_-102+16delins...
ENST00000509063.5:c.79+12_79+16delinsATTTT ENSP00000422784.1:n.79+12_79+16delinsATTT...
ENST00000510166.5:n.120+12_120+16delinsATTTT
ENST00000514786.1:n.48+82_48+86delinsATTTT
ENST00000515133.5:n.120+12_120+16delinsATTTT
ENST00000621085.4:c.79+12_79+16delinsATTTT ENSP00000483421.1:n.79+12_79+16delinsATTT...
ENST00000621628.4:c.79+12_79+16delinsATTTT ENSP00000480485.1:n.79+12_79+16delinsATTT...
NM_000477.5:c.79+12_79+16delinsATTTT NP_000468.1:n.79+12_79+16delinsATTTT
NM_000477.6:c.79+12_79+16delinsATTTT NP_000468.1:n.79+12_79+16delinsATTTT
NM_000477.7:c.79+12_79+16delinsATTTT MANE Select NP_000468.1:n.79+12_79+16delinsATTTT