Canonical Allele Identifier: CA2670966575
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73419486_73419487insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000666.2:g.73419486_73419487insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000004.11:g.74285203_74285204insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000666.1:g.74285203_74285204insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000004.10:g.74504067_74504068insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_009291.1:g.20232_20233insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000295897.4:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000295897.8:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000295897.4:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000401494.7:c.1308-21_1308-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000384695.3:n.1308-21_1308-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000415165.6:c.1077-21_1077-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000401820.2:n.1077-21_1077-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000476441.6:c.*932-21_*932-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000423727.1:n.*932-21_*932-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000486939.1:n.307-21_307-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000503124.5:c.1203-21_1203-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000421027.1:n.1203-21_1203-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000505649.5:n.1200-21_1200-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000508932.5:n.175+31_175+32insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000509063.5:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000422784.1:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000511370.1:c.1186-21_1186-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000621085.4:c.1014-21_1014-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000483421.1:n.1014-21_1014-20insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000621628.4:c.1014-21_1014-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000480485.1:n.1014-21_1014-20insTTTTTTTTTTTTTTTTTTTTTTT...
NM_000477.5:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000468.1:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_000477.6:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000468.1:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_000477.7:c.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000468.1:n.1653-21_1653-20insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT...