Canonical Allele Identifier: CA2695210699

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220811dup , CM000671.2:g.91220811dup	GRCh38
NC_000009.11:g.93983093dup , CM000671.1:g.93983093dup	GRCh37
NC_000009.10:g.93022914dup	NCBI36
NG_008017.1:g.146114dup , LRG_449:g.146114dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.837dup MANE Select	ENSP00000364883.5:p.Pro280ThrfsTer15
ENST00000303617.5:c.750dup	ENSP00000307334.5:p.Pro251ThrfsTer15
ENST00000375731.8:c.837dup	ENSP00000364883.4:p.Pro280ThrfsTer15
ENST00000473695.1:n.109dup
NM_001306190.1:c.750dup	NP_001293119.1:p.Pro251ThrfsTer15
NM_001698.2:c.837dup , LRG_449t1:c.837dup	NP_001689.1:p.Pro280ThrfsTer15
XM_005252066.2:c.867dup	XP_005252123.1:p.Pro290ThrfsTer15
XM_005252067.3:c.867dup	XP_005252124.1:p.Pro290ThrfsTer15
XM_005252069.3:c.867dup	XP_005252126.1:p.Pro290ThrfsTer?
XM_005252073.2:c.375dup	XP_005252130.1:p.Pro126ThrfsTer15
XM_006717150.2:c.780dup	XP_006717213.1:p.Pro261ThrfsTer15
XM_011518801.1:c.513dup	XP_011517103.1:p.Pro172ThrfsTer15
XM_011518802.1:c.510dup	XP_011517104.1:p.Pro171ThrfsTer15
NM_001351431.1:c.510dup	NP_001338360.1:p.Pro171ThrfsTer15
NM_001351432.1:c.510dup	NP_001338361.1:p.Pro171ThrfsTer15
NM_001351433.1:c.510dup	NP_001338362.1:p.Pro171ThrfsTer15
XM_005252066.3:c.867dup	XP_005252123.1:p.Pro290ThrfsTer15
XM_005252067.4:c.867dup	XP_005252124.1:p.Pro290ThrfsTer15
XM_005252069.4:c.867dup	XP_005252126.1:p.Pro290ThrfsTer?
XM_006717150.3:c.780dup	XP_006717213.1:p.Pro261ThrfsTer15
XM_017014849.1:c.837dup	XP_016870338.1:p.Pro280ThrfsTer15
XR_001746328.2:n.1062dup
XR_001746329.2:n.1014dup
NM_001698.3:c.837dup MANE Select	NP_001689.1:p.Pro280ThrfsTer15
NM_001306190.2:c.750dup	NP_001293119.1:p.Pro251ThrfsTer15
NM_001351431.2:c.510dup	NP_001338360.1:p.Pro171ThrfsTer15
NM_001351432.2:c.510dup	NP_001338361.1:p.Pro171ThrfsTer15
NM_001351433.2:c.510dup	NP_001338362.1:p.Pro171ThrfsTer15