Canonical Allele Identifier: CA1863689247
Gene: AUH HGNC NCBI

Linked Data

dbSNP Id: rs1827110120

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91221101_91221102del , CM000671.2:g.91221101_91221102del GRCh38
NC_000009.11:g.93983383_93983384del , CM000671.1:g.93983383_93983384del GRCh37
NC_000009.10:g.93023204_93023205del NCBI36
NG_008017.1:g.145826_145827del , LRG_449:g.145826_145827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.656-107_656-106del MANE Select ENSP00000364883.5:n.656-107_656-106del
ENST00000303617.5:c.569-107_569-106del ENSP00000307334.5:n.569-107_569-106del
ENST00000375731.8:c.656-107_656-106del ENSP00000364883.4:n.656-107_656-106del
NM_001306190.1:c.569-107_569-106del NP_001293119.1:n.569-107_569-106del
NM_001698.2:c.656-107_656-106del , LRG_449t1:c.656-107_656-106del NP_001689.1:n.656-107_656-106del
XM_005252066.2:c.686-107_686-106del XP_005252123.1:n.686-107_686-106del
XM_005252067.3:c.686-107_686-106del XP_005252124.1:n.686-107_686-106del
XM_005252069.3:c.686-107_686-106del XP_005252126.1:n.686-107_686-106del
XM_005252073.2:c.194-107_194-106del XP_005252130.1:n.194-107_194-106del
XM_006717150.2:c.599-107_599-106del XP_006717213.1:n.599-107_599-106del
XM_011518801.1:c.332-107_332-106del XP_011517103.1:n.332-107_332-106del
XM_011518802.1:c.329-107_329-106del XP_011517104.1:n.329-107_329-106del
NM_001351431.1:c.329-107_329-106del NP_001338360.1:n.329-107_329-106del
NM_001351432.1:c.329-107_329-106del NP_001338361.1:n.329-107_329-106del
NM_001351433.1:c.329-107_329-106del NP_001338362.1:n.329-107_329-106del
XM_005252066.3:c.686-107_686-106del XP_005252123.1:n.686-107_686-106del
XM_005252067.4:c.686-107_686-106del XP_005252124.1:n.686-107_686-106del
XM_005252069.4:c.686-107_686-106del XP_005252126.1:n.686-107_686-106del
XM_006717150.3:c.599-107_599-106del XP_006717213.1:n.599-107_599-106del
XM_017014849.1:c.656-107_656-106del XP_016870338.1:n.656-107_656-106del
XR_001746328.2:n.881-107_881-106del
XR_001746329.2:n.833-107_833-106del
NM_001698.3:c.656-107_656-106del MANE Select NP_001689.1:n.656-107_656-106del
NM_001306190.2:c.569-107_569-106del NP_001293119.1:n.569-107_569-106del
NM_001351431.2:c.329-107_329-106del NP_001338360.1:n.329-107_329-106del
NM_001351432.2:c.329-107_329-106del NP_001338361.1:n.329-107_329-106del
NM_001351433.2:c.329-107_329-106del NP_001338362.1:n.329-107_329-106del