Canonical Allele Identifier: CA2841137713

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91221003A>G , CM000671.2:g.91221003A>G	GRCh38
NC_000009.11:g.93983285A>G , CM000671.1:g.93983285A>G	GRCh37
NC_000009.10:g.93023106A>G	NCBI36
NG_008017.1:g.145922T>C , LRG_449:g.145922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.656-11T>C MANE Select	ENSP00000364883.5:n.656-11T>C
ENST00000303617.5:c.569-11T>C	ENSP00000307334.5:n.569-11T>C
ENST00000375731.8:c.656-11T>C	ENSP00000364883.4:n.656-11T>C
NM_001306190.1:c.569-11T>C	NP_001293119.1:n.569-11T>C
NM_001698.2:c.656-11T>C , LRG_449t1:c.656-11T>C	NP_001689.1:n.656-11T>C
XM_005252066.2:c.686-11T>C	XP_005252123.1:n.686-11T>C
XM_005252067.3:c.686-11T>C	XP_005252124.1:n.686-11T>C
XM_005252069.3:c.686-11T>C	XP_005252126.1:n.686-11T>C
XM_005252073.2:c.194-11T>C	XP_005252130.1:n.194-11T>C
XM_006717150.2:c.599-11T>C	XP_006717213.1:n.599-11T>C
XM_011518801.1:c.332-11T>C	XP_011517103.1:n.332-11T>C
XM_011518802.1:c.329-11T>C	XP_011517104.1:n.329-11T>C
NM_001351431.1:c.329-11T>C	NP_001338360.1:n.329-11T>C
NM_001351432.1:c.329-11T>C	NP_001338361.1:n.329-11T>C
NM_001351433.1:c.329-11T>C	NP_001338362.1:n.329-11T>C
XM_005252066.3:c.686-11T>C	XP_005252123.1:n.686-11T>C
XM_005252067.4:c.686-11T>C	XP_005252124.1:n.686-11T>C
XM_005252069.4:c.686-11T>C	XP_005252126.1:n.686-11T>C
XM_006717150.3:c.599-11T>C	XP_006717213.1:n.599-11T>C
XM_017014849.1:c.656-11T>C	XP_016870338.1:n.656-11T>C
XR_001746328.2:n.881-11T>C
XR_001746329.2:n.833-11T>C
NM_001698.3:c.656-11T>C MANE Select	NP_001689.1:n.656-11T>C
NM_001306190.2:c.569-11T>C	NP_001293119.1:n.569-11T>C
NM_001351431.2:c.329-11T>C	NP_001338360.1:n.329-11T>C
NM_001351432.2:c.329-11T>C	NP_001338361.1:n.329-11T>C
NM_001351433.2:c.329-11T>C	NP_001338362.1:n.329-11T>C