Canonical Allele Identifier: CA373835059

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983121T>A (hg19) ; chr9:g.91220839T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220839T>A , CM000671.2:g.91220839T>A	GRCh38
NC_000009.11:g.93983121T>A , CM000671.1:g.93983121T>A	GRCh37
NC_000009.10:g.93022942T>A	NCBI36
NG_008017.1:g.146086A>T , LRG_449:g.146086A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.809A>T MANE Select	ENSP00000364883.5:p.Lys270Met
ENST00000303617.5:c.722A>T	ENSP00000307334.5:p.Lys241Met
ENST00000375731.8:c.809A>T	ENSP00000364883.4:p.Lys270Met
ENST00000473695.1:n.81A>T
NM_001306190.1:c.722A>T	NP_001293119.1:p.Lys241Met
NM_001698.2:c.809A>T , LRG_449t1:c.809A>T	NP_001689.1:p.Lys270Met
XM_005252066.2:c.839A>T	XP_005252123.1:p.Lys280Met
XM_005252067.3:c.839A>T	XP_005252124.1:p.Lys280Met
XM_005252069.3:c.839A>T	XP_005252126.1:p.Lys280Met
XM_005252073.2:c.347A>T	XP_005252130.1:p.Lys116Met
XM_006717150.2:c.752A>T	XP_006717213.1:p.Lys251Met
XM_011518801.1:c.485A>T	XP_011517103.1:p.Lys162Met
XM_011518802.1:c.482A>T	XP_011517104.1:p.Lys161Met
NM_001351431.1:c.482A>T	NP_001338360.1:p.Lys161Met
NM_001351432.1:c.482A>T	NP_001338361.1:p.Lys161Met
NM_001351433.1:c.482A>T	NP_001338362.1:p.Lys161Met
XM_005252066.3:c.839A>T	XP_005252123.1:p.Lys280Met
XM_005252067.4:c.839A>T	XP_005252124.1:p.Lys280Met
XM_005252069.4:c.839A>T	XP_005252126.1:p.Lys280Met
XM_006717150.3:c.752A>T	XP_006717213.1:p.Lys251Met
XM_017014849.1:c.809A>T	XP_016870338.1:p.Lys270Met
XR_001746328.2:n.1034A>T
XR_001746329.2:n.986A>T
NM_001698.3:c.809A>T MANE Select	NP_001689.1:p.Lys270Met
NM_001306190.2:c.722A>T	NP_001293119.1:p.Lys241Met
NM_001351431.2:c.482A>T	NP_001338360.1:p.Lys161Met
NM_001351432.2:c.482A>T	NP_001338361.1:p.Lys161Met
NM_001351433.2:c.482A>T	NP_001338362.1:p.Lys161Met