Canonical Allele Identifier: CA589426888

Gene: AUH

Linked Data

• ClinVar Variation Id: 1444539
• ClinVar RCV Id: RCV001982466
• dbSNP Id: rs781142774
• gnomAD v2: 9-93983269-T-TC
• gnomAD v4: 9-91220987-T-TC
• MyVariant Identifiers: chr9:g.93983269_93983270insC (hg19) ; chr9:g.91220987_91220988insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220993dup , CM000671.2:g.91220993dup	GRCh38
NC_000009.11:g.93983275dup , CM000671.1:g.93983275dup	GRCh37
NC_000009.10:g.93023096dup	NCBI36
NG_008017.1:g.145937dup , LRG_449:g.145937dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.660dup
ENST00000303617.5:c.573dup
ENST00000375731.8:c.660dup
NM_001306190.1:c.573dup
NM_001698.2:c.660dup , LRG_449t1:c.660dup
XM_005252066.2:c.690dup
XM_005252067.3:c.690dup
XM_005252069.3:c.690dup
XM_005252073.2:c.198dup
XM_006717150.2:c.603dup
XM_011518801.1:c.336dup
XM_011518802.1:c.333dup
NM_001351431.1:c.333dup
NM_001351432.1:c.333dup
NM_001351433.1:c.333dup
XM_005252066.3:c.690dup
XM_005252067.4:c.690dup
XM_005252069.4:c.690dup
XM_006717150.3:c.603dup
XM_017014849.1:c.660dup
XR_001746328.2:n.885dup
XR_001746329.2:n.837dup
NM_001698.3:c.660dup
NM_001306190.2:c.573dup
NM_001351431.2:c.333dup
NM_001351432.2:c.333dup
NM_001351433.2:c.333dup