Canonical Allele Identifier: CA195893163

Gene: AUH

Linked Data

• dbSNP Id: rs781142774
• MyVariant Identifiers: chr9:g.93983270del (hg19) ; chr9:g.91220988del (hg38)

Genomic Alleles

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

Transcript Alleles

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