Canonical Allele Identifier: CA120090

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91214427T>C , CM000671.2:g.91214427T>C	GRCh38
NC_000009.11:g.93976709T>C , CM000671.1:g.93976709T>C	GRCh37
NC_000009.10:g.93016530T>C	NCBI36
NG_008017.1:g.152498A>G , LRG_449:g.152498A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001698.3:c.943-2A>G MANE Select	NP_001689.1:n.943-2A>G
ENST00000375731.9:c.943-2A>G MANE Select	ENSP00000364883.5:n.943-2A>G
NM_001306190.1:c.856-2A>G	NP_001293119.1:n.856-2A>G
NM_001306190.2:c.856-2A>G	NP_001293119.1:n.856-2A>G
NM_001351431.1:c.616-2A>G	NP_001338360.1:n.616-2A>G
NM_001351431.2:c.616-2A>G	NP_001338360.1:n.616-2A>G
NM_001351432.1:c.616-2A>G	NP_001338361.1:n.616-2A>G
NM_001351432.2:c.616-2A>G	NP_001338361.1:n.616-2A>G
NM_001351433.1:c.568-2A>G	NP_001338362.1:n.568-2A>G
NM_001351433.2:c.568-2A>G	NP_001338362.1:n.568-2A>G
NM_001698.2:c.943-2A>G , LRG_449t1:c.943-2A>G	NP_001689.1:n.943-2A>G
ENST00000303617.5:c.856-2A>G	ENSP00000307334.5:n.856-2A>G
ENST00000375731.8:c.943-2A>G	ENSP00000364883.4:n.943-2A>G
ENST00000473695.1:n.167-2A>G
XM_005252066.2:c.973-2A>G	XP_005252123.1:n.973-2A>G
XM_005252066.3:c.973-2A>G	XP_005252123.1:n.973-2A>G
XM_005252067.3:c.925-2A>G	XP_005252124.1:n.925-2A>G
XM_005252067.4:c.925-2A>G	XP_005252124.1:n.925-2A>G
XM_005252073.2:c.481-2A>G	XP_005252130.1:n.481-2A>G
XM_006717150.2:c.886-2A>G	XP_006717213.1:n.886-2A>G
XM_006717150.3:c.886-2A>G	XP_006717213.1:n.886-2A>G
XM_011518801.1:c.619-2A>G	XP_011517103.1:n.619-2A>G
XM_011518802.1:c.616-2A>G	XP_011517104.1:n.616-2A>G
XM_017014849.1:c.895-2A>G	XP_016870338.1:n.895-2A>G
XR_001746328.2:n.1168-2A>G
XR_001746329.2:n.1120-2A>G