Canonical Allele Identifier: CA2670966608

Gene: ALB

Linked Data

• gnomAD v4: 4-73419640-G-GGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419640_73419641insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA , CM000666.2:g.73419640_73419641insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	GRCh38
NC_000004.11:g.74285357_74285358insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA , CM000666.1:g.74285357_74285358insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	GRCh37
NC_000004.10:g.74504221_74504222insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	NCBI36
NG_009291.1:g.20386_20387insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA MANE Select	ENSP00000295897.4:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000295897.8:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000295897.4:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000401494.7:c.1440+1_1440+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000384695.3:n.1440+1_1440+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000415165.6:c.1209+1_1209+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000401820.2:n.1209+1_1209+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000476441.6:c.*1064+1_*1064+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000423727.1:n.*1064+1_*1064+2insGTAAAAAACTTGTTGCTGCAAGT...
ENST00000495173.1:n.93+1_93+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA
ENST00000503124.5:c.1335+1_1335+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000421027.1:n.1335+1_1335+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000505649.5:n.1332+1_1332+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA
ENST00000508932.5:n.175+185_175+186insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA
ENST00000509063.5:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000422784.1:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000511370.1:c.1318+1_1318+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA
ENST00000621085.4:c.1146+1_1146+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000483421.1:n.1146+1_1146+2insGTAAAAAACTTGTTGCTGCAAGTCA...
ENST00000621628.4:c.1146+1_1146+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	ENSP00000480485.1:n.1146+1_1146+2insGTAAAAAACTTGTTGCTGCAAGTCA...
NM_000477.5:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	NP_000468.1:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGC...
NM_000477.6:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA	NP_000468.1:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGC...
NM_000477.7:c.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGGCTTA MANE Select	NP_000468.1:n.1785+1_1785+2insGTAAAAAACTTGTTGCTGCAAGTCAAGCTGC...