Canonical Allele Identifier: CA2243897683

Gene: ASPA SPATA22

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3499452_3499453delinsCT , CM000679.2:g.3499452_3499453delinsCT	GRCh38
NC_000017.10:g.3402746_3402747delinsCT , CM000679.1:g.3402746_3402747delinsCT	GRCh37
NC_000017.9:g.3349496_3349497delinsCT	NCBI36
NG_008399.1:g.30343_30344delinsCT
NG_008399.2:g.30807_30808delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263080.3:c.*364_*365delinsCT (ASPA) MANE Select	ENSP00000263080.2:n.*364_*365delinsCT
ENST00000263080.2:c.*364_*365delinsCT (ASPA)	ENSP00000263080.2:n.*364_*365delinsCT
ENST00000541913.5:c.-74+13959_-74+13960delinsAG (SPATA22)	ENSP00000441920.1:n.-74+13959_-74+13960delinsAG
ENST00000570318.1:c.-74+14158_-74+14159delinsAG (SPATA22)	ENSP00000459147.1:n.-74+14158_-74+14159delinsAG
XM_005256829.1:c.-74+13959_-74+13960delinsAG (SPATA22)	XP_005256886.1:n.-74+13959_-74+13960delinsAG
XM_005256830.1:c.-74+13959_-74+13960delinsAG (SPATA22)	XP_005256887.1:n.-74+13959_-74+13960delinsAG
NM_001321336.1:c.-74+13959_-74+13960delinsAG (SPATA22)	NP_001308265.1:n.-74+13959_-74+13960delinsAG
NM_001321337.1:c.-74+13959_-74+13960delinsAG (SPATA22)	NP_001308266.1:n.-74+13959_-74+13960delinsAG
XM_017024661.1:c.*364_*365delinsCT (ASPA)	XP_016880150.1:n.*364_*365delinsCT
XM_024450764.1:c.*364_*365delinsCT (ASPA)	XP_024306532.1:n.*364_*365delinsCT
NM_000049.3:c.*364_*365delinsCT (ASPA)	NP_000040.1:n.*364_*365delinsCT
NM_000049.4:c.*364_*365delinsCT (ASPA) MANE Select	NP_000040.1:n.*364_*365delinsCT
NM_001321336.2:c.-74+13959_-74+13960delinsAG (SPATA22)	NP_001308265.1:n.-74+13959_-74+13960delinsAG
NM_001321337.2:c.-74+13959_-74+13960delinsAG (SPATA22)	NP_001308266.1:n.-74+13959_-74+13960delinsAG