Canonical Allele Identifier: CA589432986

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91217268G>T , CM000671.2:g.91217268G>T	GRCh38
NC_000009.11:g.93979550G>T , CM000671.1:g.93979550G>T	GRCh37
NC_000009.10:g.93019371G>T	NCBI36
NG_008017.1:g.149657C>A , LRG_449:g.149657C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001698.3:c.894+9C>A MANE Select	NP_001689.1:n.894+9C>A
ENST00000375731.9:c.894+9C>A MANE Select	ENSP00000364883.5:n.894+9C>A
NM_001306190.1:c.807+9C>A	NP_001293119.1:n.807+9C>A
NM_001306190.2:c.807+9C>A	NP_001293119.1:n.807+9C>A
NM_001351431.1:c.567+9C>A	NP_001338360.1:n.567+9C>A
NM_001351431.2:c.567+9C>A	NP_001338360.1:n.567+9C>A
NM_001351432.1:c.567+9C>A	NP_001338361.1:n.567+9C>A
NM_001351432.2:c.567+9C>A	NP_001338361.1:n.567+9C>A
NM_001351433.1:c.567+9C>A	NP_001338362.1:n.567+9C>A
NM_001351433.2:c.567+9C>A	NP_001338362.1:n.567+9C>A
NM_001698.2:c.894+9C>A , LRG_449t1:c.894+9C>A	NP_001689.1:n.894+9C>A
ENST00000303617.5:c.807+9C>A	ENSP00000307334.5:n.807+9C>A
ENST00000375731.8:c.894+9C>A	ENSP00000364883.4:n.894+9C>A
ENST00000473695.1:n.166+9C>A
XM_005252066.2:c.924+9C>A	XP_005252123.1:n.924+9C>A
XM_005252066.3:c.924+9C>A	XP_005252123.1:n.924+9C>A
XM_005252067.3:c.924+9C>A	XP_005252124.1:n.924+9C>A
XM_005252067.4:c.924+9C>A	XP_005252124.1:n.924+9C>A
XM_005252073.2:c.432+9C>A	XP_005252130.1:n.432+9C>A
XM_006717150.2:c.837+9C>A	XP_006717213.1:n.837+9C>A
XM_006717150.3:c.837+9C>A	XP_006717213.1:n.837+9C>A
XM_011518801.1:c.570+9C>A	XP_011517103.1:n.570+9C>A
XM_011518802.1:c.567+9C>A	XP_011517104.1:n.567+9C>A
XM_017014849.1:c.894+9C>A	XP_016870338.1:n.894+9C>A
XR_001746328.2:n.1119+9C>A
XR_001746329.2:n.1071+9C>A