Canonical Allele Identifier: CA373835308

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983238G>C (hg19) ; chr9:g.91220956G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220956G>C , CM000671.2:g.91220956G>C	GRCh38
NC_000009.11:g.93983238G>C , CM000671.1:g.93983238G>C	GRCh37
NC_000009.10:g.93023059G>C	NCBI36
NG_008017.1:g.145969C>G , LRG_449:g.145969C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.692C>G MANE Select	ENSP00000364883.5:p.Ser231Cys
ENST00000303617.5:c.605C>G	ENSP00000307334.5:p.Ser202Cys
ENST00000375731.8:c.692C>G	ENSP00000364883.4:p.Ser231Cys
NM_001306190.1:c.605C>G	NP_001293119.1:p.Ser202Cys
NM_001698.2:c.692C>G , LRG_449t1:c.692C>G	NP_001689.1:p.Ser231Cys
XM_005252066.2:c.722C>G	XP_005252123.1:p.Ser241Cys
XM_005252067.3:c.722C>G	XP_005252124.1:p.Ser241Cys
XM_005252069.3:c.722C>G	XP_005252126.1:p.Ser241Cys
XM_005252073.2:c.230C>G	XP_005252130.1:p.Ser77Cys
XM_006717150.2:c.635C>G	XP_006717213.1:p.Ser212Cys
XM_011518801.1:c.368C>G	XP_011517103.1:p.Ser123Cys
XM_011518802.1:c.365C>G	XP_011517104.1:p.Ser122Cys
NM_001351431.1:c.365C>G	NP_001338360.1:p.Ser122Cys
NM_001351432.1:c.365C>G	NP_001338361.1:p.Ser122Cys
NM_001351433.1:c.365C>G	NP_001338362.1:p.Ser122Cys
XM_005252066.3:c.722C>G	XP_005252123.1:p.Ser241Cys
XM_005252067.4:c.722C>G	XP_005252124.1:p.Ser241Cys
XM_005252069.4:c.722C>G	XP_005252126.1:p.Ser241Cys
XM_006717150.3:c.635C>G	XP_006717213.1:p.Ser212Cys
XM_017014849.1:c.692C>G	XP_016870338.1:p.Ser231Cys
XR_001746328.2:n.917C>G
XR_001746329.2:n.869C>G
NM_001698.3:c.692C>G MANE Select	NP_001689.1:p.Ser231Cys
NM_001306190.2:c.605C>G	NP_001293119.1:p.Ser202Cys
NM_001351431.2:c.365C>G	NP_001338360.1:p.Ser122Cys
NM_001351432.2:c.365C>G	NP_001338361.1:p.Ser122Cys
NM_001351433.2:c.365C>G	NP_001338362.1:p.Ser122Cys