Canonical Allele Identifier: CA1863689159
Gene: AUH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91220992_91220994delinsCCT , CM000671.2:g.91220992_91220994delinsCCT GRCh38
NC_000009.11:g.93983274_93983276delinsCCT , CM000671.1:g.93983274_93983276delinsCCT GRCh37
NC_000009.10:g.93023095_93023097delinsCCT NCBI36
NG_008017.1:g.145931_145933delinsAGG , LRG_449:g.145931_145933delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.656-2_656delinsAGG
ENST00000303617.5:c.569-2_569delinsAGG
ENST00000375731.8:c.656-2_656delinsAGG
NM_001306190.1:c.569-2_569delinsAGG
NM_001698.2:c.656-2_656delinsAGG , LRG_449t1:c.656-2_656delinsAGG
XM_005252066.2:c.686-2_686delinsAGG
XM_005252067.3:c.686-2_686delinsAGG
XM_005252069.3:c.686-2_686delinsAGG
XM_005252073.2:c.194-2_194delinsAGG
XM_006717150.2:c.599-2_599delinsAGG
XM_011518801.1:c.332-2_332delinsAGG
XM_011518802.1:c.329-2_329delinsAGG
NM_001351431.1:c.329-2_329delinsAGG
NM_001351432.1:c.329-2_329delinsAGG
NM_001351433.1:c.329-2_329delinsAGG
XM_005252066.3:c.686-2_686delinsAGG
XM_005252067.4:c.686-2_686delinsAGG
XM_005252069.4:c.686-2_686delinsAGG
XM_006717150.3:c.599-2_599delinsAGG
XM_017014849.1:c.656-2_656delinsAGG
XR_001746328.2:n.881-2_881delinsAGG
XR_001746329.2:n.833-2_833delinsAGG
NM_001698.3:c.656-2_656delinsAGG
NM_001306190.2:c.569-2_569delinsAGG
NM_001351431.2:c.329-2_329delinsAGG
NM_001351432.2:c.329-2_329delinsAGG
NM_001351433.2:c.329-2_329delinsAGG